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吡唑

    级别和纯度:
  • ≥98%(GC)
有货

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货号 (SKU) 包装规格 是否现货 价格 数量
P100994-25g
25g 现货 Stock Image
P100994-100g
100g 现货 Stock Image
P100994-500g
500g 现货 Stock Image
P100994-1kg
1kg 现货 Stock Image

基本描述

别名 1,2-二氮唑 | 邻二氮杂茂 | 二氮二烯五环 | 1H-吡唑
英文别名 1,2-Diazole
规格或纯度 ≥98%(GC)
英文名称 Pyrazole
储存温度 充氩
运输条件 常规运输
产品介绍

溶于水,溶于醇、醚和苯。 用作制备有机金属化和物的配体。


纯度 ≥98%(GC)

关联靶点(人)

TBXAS1 Tchem Thromboxane-A synthase (3355 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
CYP2A6 Tchem Cytochrome P450 2A6 (2861 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
A498 (42825 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
ACHN (49357 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
CCRF-CEM (65223 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
COLO 205 (50209 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
HL-60 (67320 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
HT-29 (80576 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
K562 (73714 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
KM12 (47707 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
MCF7 (126967 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
MOLT-4 (49676 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
OVCAR-3 (48710 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
OVCAR-4 (44535 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
OVCAR-8 (47708 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
PC-3 (62116 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
RPMI-8226 (44974 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
RXF 393 (41971 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SF-295 (48000 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SK-MEL-2 (46422 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SK-MEL-28 (48833 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SK-MEL-5 (47095 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SK-OV-3 (52876 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SN12C (47755 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SNB-19 (46794 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
TK-10 (45540 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
U-251 (51189 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
UACC-62 (47335 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
UO-31 (46270 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
786-0 (47912 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
A549 (127892 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
NCI/ADR-RES (33767 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
T47D (39041 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
EKVX (44102 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
NCI-H322M (45589 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
HCC 2998 (41480 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
HCT-116 (91556 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
HOP-92 (41141 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
Hs-578T (29457 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
NCI-H460 (60772 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SF-268 (49410 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
IGROV-1 (47897 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
LOX IMVI (44321 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
HOP-62 (47048 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
MDA-MB-435 (38290 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
MDA-N (28205 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
Malme-3M (44254 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
SNB-75 (44215 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
NCI-H226 (44470 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID
NCI-H23 (49055 活性数据)
活性类型 Relation Activity value Units Action Type 期刊 PubMed Id doi Assay Aladdin ID

作用机制

作用机制 Action Type target ID Target Name Target Type Target Organism Binding Site Name 参考文献

名称和识别符

PubChem SID 488179594
EC号 206-017-1
分子类型 小分子
IIUPAC Name 1H-pyrazole
INCHI 1S/C3H4N2/c1-2-4-5-3-1/h1-3H,(H,4,5)
InChi Key WTKZEGDFNFYCGP-UHFFFAOYSA-N
Smiles C1=CNN=C1
Isomeric SMILES C1=CNN=C1
分子量 68.08
Beilstein号 103775
Reaxy-Rn 103775
Reaxys-RN link address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=103775&ln=

化学和物理性质

溶解性 Soluble in water.
密度 1.1147
敏感性 易吸潮,对空气敏感
沸点 186-188°C
熔点 67-70°C
分子量 68.080 g/mol
XLogP3 0.300
氢键供体数Hydrogen Bond Donor Count 1
氢键受体数Hydrogen Bond Acceptor Count 1
可旋转键计数Rotatable Bond Count 0
精确质量Exact Mass 68.0374 Da
单同位素质量Monoisotopic Mass 68.0374 Da
拓扑极表面积Topological Polar Surface Area 28.700 Ų
重原子数Heavy Atom Count 5
形式电荷Formal Charge 0
复杂度Complexity 28.100
同位素原子数Isotope Atom Count 0
定义的原子立体中心计数Defined Atom Stereocenter Count 0
未定义的原子立体中心计数Undefined Atom Stereocenter Count 0
定义的键立体中心计数Defined Bond Stereocenter Count 0
未定义的键立体中心计数Undefined Bond Stereocenter Count 0
所有立体化学键的总数The total count of all stereochemical bonds 0
共价键合单元计数Covalently-Bonded Unit Count 1

安全和危险性(GHS)

象形图 GHS05,   GHS06,   GHS07,   GHS08
信号词 危险
危险声明

H302: 吞食有害

H311: 皮肤接触有毒

H315: 引起皮肤刺激

H318: 造成严重的眼睛损伤

H319: 引起严重眼睛刺激

H335: 可能引起呼吸道刺激

H372: 通过长时间或反复暴露对器官造成损害

H412: 对水生生物有害并具有长期持续影响

预防措施声明

P260: 不要吸入灰尘/烟雾/气体/雾/蒸汽/喷雾。

P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾

P264: 处理后要彻底洗手。

P270: 使用本产品时,请勿进食、饮水或吸烟。

P271: 仅在室外或通风良好的地方使用。

P273: 避免释放到环境中。

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P321: 特殊处理(请参阅此标签上的...)。

P330: 漱口

P302+P352: 如皮肤沾染:用水充分清洗。

P304+P340: 如误吸入:将人转移到空气新鲜处,保持呼吸舒适体位。

P305+P351+P338: 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。

P361+P364: 立即脱掉所有沾染的衣服,清洗后方可重新使用。

P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。

P405: 密闭存放

P403+P233: 存放在通风良好的地方。保持容器密闭。

P501: 将内容物/容器处理到。。。

P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。

P301+P317: 如果被吞咽:请寻求医疗帮助。

P305+P354+P338: 如果进入眼睛:立即用水冲洗几分钟。取下隐形眼镜(如果有的话),并且操作简单。继续冲洗。

P317: 寻求紧急医疗救助。

P337+P317: 如果眼睛刺激持续:寻求医疗帮助。

P332+P317: 如果出现皮肤刺激:请寻求医疗帮助。

P316: 立即寻求紧急医疗救助。

P319: 如果你感到不适,请寻求医疗帮助。

WGK Germany 1
RTECS UQ4900000
Merck Index 7960
个人防护装备 dust mask type N95 (US),Eyeshields,Gloves

质检证书(CoA,COO,BSE/TSE 和分析图谱)

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找到23个结果

批号(Lot Number) 证书类型 货号
L2217058 分析证书 P100994
L2217060 分析证书 P100994
L2426533 分析证书 P100994
L2426535 分析证书 P100994
L2426524 分析证书 P100994
L2426525 分析证书 P100994
G2426201 分析证书 P100994
G2426199 分析证书 P100994
G2426200 分析证书 P100994
I2103236 分析证书 P100994
I2103237 分析证书 P100994
D2417428 分析证书 P100994
D2417432 分析证书 P100994
H1807103 分析证书 P100994
C2414697 分析证书 P100994
B24231062 分析证书 P100994
B24231063 分析证书 P100994
B24231064 分析证书 P100994
D2020146 分析证书 P100994
L2217035 分析证书 P100994
L2217059 分析证书 P100994
L2217102 分析证书 P100994
K2313132 分析证书 P100994

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此产品的引用文献

引用文献

1. Michael Hirtz,Naresh Kumar,Jörn-Holger Franke,Juanyuan Hao,Nan Lu,Harald Fuchs,Lifeng Chi.  (2012-10-10)  Selective deposition of organic molecules onto DPPC templates--a molecular dynamics study..  Journal of colloid and interface science,  389  ((1)): (206-212).  [PMID:23044270]
2. Ke-Ming Qiu,Ru Yan,Man Xing,Hai-Hong Wang,Hong-En Cui,Hai-Bin Gong,Hai-Liang Zhu.  (2012-10-16)  Synthesis, biological evaluation and molecular modeling of dihydro-pyrazolyl-thiazolinone derivatives as potential COX-2 inhibitors..  Bioorganic & medicinal chemistry,  20  ((22)): (6648-6654).  [PMID:23062711]
3. James S Scott,Joanne deSchoolmeester,Elaine Kilgour,Rachel M Mayers,Martin J Packer,David Hargreaves,Stefan Gerhardt,Derek J Ogg,Amanda Rees,Nidhal Selmi,Andrew Stocker,John G Swales,Paul R O Whittamore.  (2012-10-24)  Novel acidic 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor with reduced acyl glucuronide liability: the discovery of 4-[4-(2-adamantylcarbamoyl)-5-tert-butyl-pyrazol-1-yl]benzoic acid (AZD8329)..  Journal of medicinal chemistry,  55  ((22)): (10136-10147).  [PMID:23088558]
4. Tiphaine Rogez-Florent,Samuel Meignan,Catherine Foulon,Perrine Six,Abigaëlle Gros,Christine Bal-Mahieu,Claudiu T Supuran,Andrea Scozzafava,Raphaël Frédérick,Bernard Masereel,Patrick Depreux,Amélie Lansiaux,Jean-François Goossens,Sébastien Gluszok,Laurence Goossens.  (2012-11-22)  New selective carbonic anhydrase IX inhibitors: synthesis and pharmacological evaluation of diarylpyrazole-benzenesulfonamides..  Bioorganic & medicinal chemistry,  21  ((6)): (1451-1464).  [PMID:23168081]
5. Ishita Banerjee,Pabitra Narayan Samanta,Kalyan Kumar Das,Rodica Ababei,Marguerite Kalisz,Adrien Girard,Corine Mathonière,M Nethaji,Rodolphe Clérac,Mahammad Ali.  (2012-11-23)  Air oxygenation chemistry of 4-TBC catalyzed by chloro bridged dinuclear copper(II) complexes of pyrazole based tridentate ligands: synthesis, structure, magnetic and computational studies..  Dalton transactions (Cambridge, England : 2003),  42  ((5)): (1879-1892).  [PMID:23172025]
6. Kentaro Futatsugi,Vincent Mascitti,Cristiano R W Guimarães,Nao Morishita,Cuiman Cai,Michael P DeNinno,Hua Gao,Michael D Hamilton,Richard Hank,Anthony R Harris,Daniel W Kung,Sophie Y Lavergne,Bruce A Lefker,Michael G Lopaze,Kim F McClure,Michael J Munchhof,Cathy Preville,Ralph P Robinson,Stephen W Wright,Paul D Bonin,Peter Cornelius,Yue Chen,Amit S Kalgutkar.  (2012-11-28)  From partial to full agonism: identification of a novel 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole as a full agonist of the human GPR119 receptor..  Bioorganic & medicinal chemistry letters,  23  ((1)): (194-197).  [PMID:23177788]
7. John R Cubanski,Scott A Cameron,James D Crowley,Allan G Blackman.  (2012-11-30)  Low symmetry pyrazole-based tripodal tetraamine ligands: metal complexes and ligand decomposition reactions..  Dalton transactions (Cambridge, England : 2003),  42  ((6)): (2174-2185).  [PMID:23192397]
8. Partha Basu,Brian W Kail,Andrew K Adams,Victor N Nemykin.  (2012-12-06)  Quantitation of the ligand effect in oxo-transfer reactions of dioxo-Mo(VI) trispyrazolyl borate complexes..  Dalton transactions (Cambridge, England : 2003),  42  ((9)): (3071-3081).  [PMID:23212540]
9. Mingzhen Mao,Yuxin Li,Qiaoxia Liu,Yunyun Zhou,Xiulan Zhang,Lixia Xiong,Yongqiang Li,Zhengming Li.  (2012-12-12)  Synthesis and insecticidal evaluation of novel N-pyridylpyrazolecarboxamides containing cyano substituent in the ortho-position..  Bioorganic & medicinal chemistry letters,  23  ((1)): (42-46).  [PMID:23218717]
10. Liao-Yuan Yao,Zheng-Su Yu,Lin Qin,Yi-Zhi Li,Yu Qin,Shu-Yan Yu.  (2012-12-22)  Self-assembly of metallomacrocycles with dipyrazole ligands and anion sensing of [Pd4Fe2] macrocycle with ferrocene-based dipyrazole ligand..  Dalton transactions (Cambridge, England : 2003),  42  ((10)): (3447-3454).  [PMID:23258755]
11. Babasaheb P Bandgar,Hemant V Chavan,Laxman K Adsul,Vishnu N Thakare,Sadanand N Shringare,Rafik Shaikh,Rajesh N Gacche.  (2013-01-08)  Design, synthesis, characterization and biological evaluation of novel pyrazole integrated benzophenones..  Bioorganic & medicinal chemistry letters,  23  ((3)): (912-916).  [PMID:23290048]
12. Xinfang Xu,Peter Y Zavalij,Wenhao Hu,Michael P Doyle.  (2013-01-11)  Vinylogous reactivity of enol diazoacetates with donor-acceptor substituted hydrazones. Synthesis of substituted pyrazole derivatives..  The Journal of organic chemistry,  78  ((4)): (1583-1588).  [PMID:23301562]
13. Kavitha Swaminathan,Dahn L Clemens,Aparajita Dey.  (2013-01-29)  Inhibition of CYP2E1 leads to decreased malondialdehyde-acetaldehyde adduct formation in VL-17A cells under chronic alcohol exposure..  Life sciences,  92  ((6-7)): (325-336).  [PMID:23352969]
14. Liqun Shen,Suyu Huang,Yuanmei Nie,Fuhou Lei.  (2013-01-29)  An efficient microwave-assisted Suzuki reaction using a new pyridine-pyrazole/Pd(II) species as catalyst in aqueous media..  Molecules (Basel, Switzerland),  18  ((2)): (1602-1612).  [PMID:23353128]
15. Maria Letizia Barreca,Giuseppe Manfroni,Pieter Leyssen,Johan Winquist,Neerja Kaushik-Basu,Jan Paeshuyse,Ramalingam Krishnan,Nunzio Iraci,Stefano Sabatini,Oriana Tabarrini,Amartya Basu,U Helena Danielson,Johan Neyts,Violetta Cecchetti.  (2013-02-16)  Structure-based discovery of pyrazolobenzothiazine derivatives as inhibitors of hepatitis C virus replication..  Journal of medicinal chemistry,  56  ((6)): (2270-2282).  [PMID:23409936]
16. Heather J Finlay,Ji Jiang,Yolanda Caringal,Alexander Kover,Mary Lee Conder,Dezhi Xing,Paul Levesque,Timothy Harper,Mei Mann Hsueh,Karnail Atwal,Michael Blanar,Ruth Wexler,John Lloyd.  (2013-02-19)  Triazolo and imidazo dihydropyrazolopyrimidine potassium channel antagonists..  Bioorganic & medicinal chemistry letters,  23  ((6)): (1743-1747).  [PMID:23414837]
17. Roberta Zaninetti,Salvatore V Cortese,Silvio Aprile,Alberto Massarotti,Pier Luigi Canonico,Giovanni Sorba,Giorgio Grosa,Armando A Genazzani,Tracey Pirali.  (2013-02-26)  A concise synthesis of pyrazole analogues of combretastatin A1 as potent anti-tubulin agents..  ChemMedChem,  ((4)): (633-643).  [PMID:23436706]
18. Kavitha Swaminathan,S Mathan Kumar,Dahn L Clemens,Aparajita Dey.  (2013-05-28)  Inhibition of CYP2E1 leads to decreased advanced glycated end product formation in high glucose treated ADH and CYP2E1 over-expressing VL-17A cells..  Biochimica et biophysica acta,  1830  ((10)): (4407-4416).  [PMID:23707663]
19. Haresh Sivaram,Jackie Tan,Han Vinh Huynh.  (2013-07-19)  Cationic gold(I) heteroleptic complexes bearing a pyrazole-derived N-heterocyclic carbene: syntheses, characterizations, and cytotoxic activities..  Dalton transactions (Cambridge, England : 2003),  42  ((34)): (12421-12428).  [PMID:23860905]
20. Javeed Ahmad Sheikh,Himanshu Sekhar Jena,Amit Adhikary,Sajal Khatua,Sanjit Konar.  (2013-08-16)  An unprecedented octadecanuclear copper(II) pyrazolate-phosphonate nanocage: synthetic, structural, magnetic, and mechanistic study..  Inorganic chemistry,  52  ((17)): (9717-9719).  [PMID:23944174]
21. Wen Liu,Mei-Juan Cai,Jin-Xing Wang,Xiao-Fan Zhao.  (2014-02-13)  In a nongenomic action, steroid hormone 20-hydroxyecdysone induces phosphorylation of cyclin-dependent kinase 10 to promote gene transcription..  Endocrinology,  155  ((5)): (1738-1750).  [PMID:24517229]
22. Changchun Cai,Hai Huang,Sean Whelan,Li Liu,Benjamin Kautza,Jason Luciano,Guoliang Wang,Guoqiang Chen,Sladjana Stratimirovic,Allan Tsung,Timothy R Billiar,Brian S Zuckerbraun.  (2014-05-07)  Benzyl alcohol attenuates acetaminophen-induced acute liver injury in a Toll-like receptor-4-dependent pattern in mice..  Hepatology (Baltimore, Md.),  60  ((3)): (990-1002).  [PMID:24798499]
23. Enas M Ahmed,Shohda A EL-Maraghy,Zakaria A Teleb,Amira A Shaheen.  (2014-06-03)  Pretreatment with turmeric modulates the inhibitory influence of cisplatin and paclitaxel on CYP2E1 and CYP3A1/2 in isolated rat hepatic microsomes..  Chemico-biological interactions,  220  (25-32).  [PMID:24882083]
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25. Beatriz Apellániz,Edurne Rujas,Pablo Carravilla,José Requejo-Isidro,Nerea Huarte,Carmen Domene,José L Nieva.  (2014-09-12)  Cholesterol-dependent membrane fusion induced by the gp41 membrane-proximal external region-transmembrane domain connection suggests a mechanism for broad HIV-1 neutralization..  Journal of virology,  88  ((22)): (13367-13377).  [PMID:25210180]
26. Ana Cristina Martínez,Medardo Hernández,Susana Novella,María Pilar Martínez,Rosa María Pagán,Carlos Hermenegildo,Albino García-Sacristán,Dolores Prieto,Sara Benedito.  (2014-09-13)  Diminished neurogenic femoral artery vasoconstrictor response in a Zucker obese rat model: differential regulation of NOS and COX derivatives..  PloS one,  ((9)): (e106372-e106372).  [PMID:25216050]
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