2-溴萘

4篇引用文献

COA

级别和纯度:

≥98%

CAS编号: 580-13-2
分子式: C₁₀H₇Br
分子量: 207.07
Beilstein号: 1858110
EC号: 209-452-5
MDL号: MFCD00004051
PubChem编号: 11372
PubChem SID: 488181318

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货号 (SKU)	包装规格	是否现货
B122362-5g	5g	现货
B122362-10g	10g	现货
B122362-25g	25g	现货
B122362-100g	100g	现货
B122362-500g	500g	现货

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芳基卤 (氟化物除外) (243) 非杂环砌块 (8221)

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基本描述

别名	2-溴代萘 \| 2-溴化萘 \| β-溴萘
英文别名	Z166622678 \| AKOS000121092 \| Q27289466 \| Naphthalene, 2-bromo- \| MFCD00004051 \| 2-BROMONAPHTHALENE \| 2-Bromo-naphthalene \| 2-bromonaphtalene \| DTXSID3060378 \| 2-Bromonaphthalene, 97% \| B0619 \| STR03261 \| BDBM50159272 \| NSC 4011 \| 2-BROMO NAPHTHALCNE \| bet
规格或纯度	≥98%
英文名称	2-Bromonaphthalene
应用	2-Bromonaphthalene was used in the synthesis of biaryls via Suzuki cross coupling reaction in water under microwave irradiation.
运输条件	常规运输
产品介绍	Reaction of 2-bromonaphthalene with cuprous cyanide in N-methylpyrrolidone has been investigated.Nanosecond time-resolved resonance Raman spectra of the T1→Tn transition of 2-bromonaphthalene in methanol solvent has been investigated.2-Bromonaphthalene was used in the synthesis of biaryls via Suzuki cross coupling reaction in water under microwave irradiation. Reaction of 2-bromonaphthalene with cuprous cyanide in N-methylpyrrolidone has been investigated.Nanosecond time-resolved resonance Raman spectra of the T1→Tn transition of 2-bromonaphthalene in methanol solvent has been investigated. 2-Bromonaphthalene was used in the synthesis of biaryls via Suzuki cross coupling reaction in water under microwave irradiation.
纯度	≥98%

关联靶点（人）

CYP2A6 Tchem 细胞色素 P450 2A6(Cytochrome P450 2A6) (2 活性数据)

点击查看靶蛋白信息： CYP2A6

活性类型	活性值-log(M)	作用机制	期刊	参考文献(PubMed IDs)

CYP2A6 Tchem Cytochrome P450 2A6 (2861 活性数据)

点击查看靶蛋白信息： CYP2A6

活性类型	Relation	Activity value	Units	Action Type	期刊	PubMed Id	doi	Assay Aladdin ID

关联靶点（其它种属）

Cyp2a5 Cytochrome P450 2A5 (126 活性数据)

点击查看靶蛋白信息： Cyp2a5

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	488181318
EC号	209-452-5
分子类型	小分子
IIUPAC Name	2-bromonaphthalene
INCHI	1S/C10H7Br/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
InChi Key	APSMUYYLXZULMS-UHFFFAOYSA-N
Smiles	C1=CC=C2C=C(C=CC2=C1)Br
Isomeric SMILES	C1=CC=C2C=C(C=CC2=C1)Br
分子量	207.07
Beilstein号	1858110
Reaxy-Rn	1858110
Reaxys-RN link address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1858110&ln=

化学和物理性质

溶解性	Slightly soluble in water.
密度	1.605
闪点(℉)	235.4 °F
闪点(℃)	112°(233°F)
沸点	281～282°C
熔点	54-58°C
分子量	207.070 g/mol
XLogP3	4.200
氢键供体数Hydrogen Bond Donor Count	0
氢键受体数Hydrogen Bond Acceptor Count	0
可旋转键计数Rotatable Bond Count	0
精确质量Exact Mass	205.973 Da
单同位素质量Monoisotopic Mass	205.973 Da
拓扑极表面积Topological Polar Surface Area	0.000 Å²
重原子数Heavy Atom Count	11
形式电荷Formal Charge	0
复杂度Complexity	133.000
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	GHS07
信号词	警告
危险声明	H302: 吞食有害 H319: 引起严重眼睛刺激
预防措施声明	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。 P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P330: 漱口 P301+P312: 如误吞咽：如感觉不适，呼叫急救中心/医生。 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。 P337+P313: 如仍觉眼刺激：求医/就诊。 P501: 将内容物/容器处理到。。。
WGK Germany	3
Merck Index	1426
个人防护装备	dust mask type N95 (US), Eyeshields, Gloves

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C of A & Other Certificates(BSE/TSE, COO):

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找到14个结果

批号(Lot Number)	证书类型	货号
C2222302	分析证书	B122362
C2222304	分析证书	B122362
C2222308	分析证书	B122362
I2319051	分析证书	B122362
E2326245	分析证书	B122362
E2326239	分析证书	B122362
H2518182	分析证书	B122362
I2501742	分析证书	B122362
I2215074	分析证书	B122362
I2215560	分析证书	B122362
I2215561	分析证书	B122362
I2215562	分析证书	B122362
F2104060	分析证书	B122362
C2222305	分析证书	B122362

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引用文献

1. Minna Rahnasto,Hannu Raunio,Antti Poso,Carsten Wittekindt,Risto O Juvonen. (2005-01-22) Quantitative structure-activity relationship analysis of inhibitors of the nicotine metabolizing CYP2A6 enzyme.. Journal of medicinal chemistry, 48 ((2)): (440-449). [PMID:15658857]
2. Kunal Roy,Partha Pratim Roy. (2008-12-27) Exploring QSAR and QAAR for inhibitors of cytochrome P450 2A6 and 2A5 enzymes using GFA and G/PLS techniques.. European journal of medicinal chemistry, 44 ((5)): (1941-1951). [PMID:19110342]
3. J M Shoulder,E L Ashenafi,C M Breneman,M C Nyman. (2019-03-22) Substituted naphthalene reaction rates with peroxy-acid treatment: prediction of reactivity using PEST.. SAR and QSAR in environmental research, 30 ((4)): (229-245). [PMID:30895805]
4. Isaiah R Speight,Timothy P Hanusa. (2020-02-06) Exploration of Mechanochemical Activation in Solid-State Fluoro-Grignard Reactions.. Molecules (Basel, Switzerland), 25 ((3)): [PMID:32012963]
5. Wei He, Xiya Yang, Jialong Duan, Junshuai Zhang, Qiyao Guo, Hao Huang, Qunwei Tang. (2023) Liquid buried interface to slide lattice and heal defects in inorganic perovskite solar cells. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 646 (695). [PMID:37229987] [10.1016/j.jcis.2023.05.135]
6. Qiyao Guo, Jialong Duan, Junshuai Zhang, Qiaoyu Zhang, Yanyan Duan, Xiya Yang, Benlin He, Yuanyuan Zhao, Qunwei Tang. (2022) Universal Dynamic Liquid Interface for Healing Perovskite Solar Cells. ADVANCED MATERIALS, 34 (26): (2202301). [PMID:35460143] [10.1002/adma.202202301]
7. Qinrui Fu, Yuan Meng, Zilin Fang, Quanqin Hu, Liang Xu, Wenhua Gao, Xiaochun Huang, Qiao Xue, Ya-Ping Sun, Fushen Lu. (2017) Boron Nitride Nanosheet-Anchored Pd–Fe Core–Shell Nanoparticles as Highly Efficient Catalysts for Suzuki–Miyaura Coupling Reactions. ACS Applied Materials & Interfaces, 9 (3): (2469–2476). [PMID:28051299] [10.1021/acsami.6b13570]
8. Xiang Han, Lei Zhao, Dong-En Wang, Juan Xu, Longlong Zhang, Mao-Sen Yuan, Qin Tu, Jinyi Wang. (2016) A TBET-based ratiometric probe for Au3+ and its application in living cells. ANALYST, 141 (3): (1098-1104). [PMID:26662283] [10.1039/C5AN01932J]

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