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苯并[b]噻吩-3-甲醛

    级别和纯度:
  • ≥98%(GC)
有货

库存信息

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库存信息

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库存信息

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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
B152938-250mg
250mg 现货 Stock Image
B152938-1g
1g 现货 Stock Image
B152938-5g
5g 现货 Stock Image
B152938-25g
25g 现货 Stock Image

基本描述

别名 苯并噻酚-3-甲醛 | 3-甲酰基苯并[b]噻吩 | 硫茚-3-甲醛
英文别名 88C6MH2ME3 | benzo[b]thiophene-3-aldehyde | NSC18872 | NSC-18872 | A1717 | F0001-1398 | 3-formylbenzothiophene | B4086 | SCHEMBL40953 | UNII-88C6MH2ME3 | benzo[b]thiophene-3-carbaldehyde | WDJLPQCBTBZTRH-UHFFFAOYSA-N | 1-benzothiophene-3-carbaldehyde | be
规格或纯度 ≥98%(GC)
英文名称 Benzo[b]thiophene-3-carboxaldehyde
储存温度 2-8°C储存,充氩
运输条件 冰袋运输
产品介绍

Thianaphthene-3-carboxaldehyde, also known as benzo[b]thiophene-3-carboxaldehyde, can be synthesized from 3-methyl-benzo[b]thiophene. It undergoes phosphine-free palladium coupling with aryl halides to form 2-arylbenzo[b]thiophenes.Thianaphthene-3-carboxaldehyde (Benzo[b]thiophene-3-carboxaldehyde) may be used as a starting material in the multi-step synthesis of anthra[2,3-b:7,6-b′]bis[1benzothiophenes (ABBTs). It may be used in the synthesis of : · 6-(N,N-dimethylamino)-2-(benzo[b]thiophen-3-yl)quinazolin-4-one · 6-(pyrrolidin-1-yl)-2-(benzo[b]thiophen-3-yl)quinazolin-4-one · (Z)-2-(benzo-[b]-thio-phen-3-yl-methyl-ene)-1-aza-bi-cyclo-[2.2.2]-octan-3-one

Thianaphthene-3-carboxaldehyde, also known as benzo[b]thiophene-3-carboxaldehyde, can be synthesized from 3-methyl-benzo[b]thiophene. It undergoes phosphine-free palladium coupling with aryl halides to form 2-arylbenzo[b]thiophenes.

纯度 ≥98%(GC)

关联靶点(人)

CYP2A6 Tchem 细胞色素 P450 2A6(Cytochrome P450 2A6) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
SLC6A1 Tclin GABA transporter 1 (308 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

关联靶点(其它种属)

Iap Intestinal alkaline phosphatase (419 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 504757960
分子类型 小分子
IIUPAC Name 1-benzothiophene-3-carbaldehyde
INCHI 1S/C9H6OS/c10-5-7-6-11-9-4-2-1-3-8(7)9/h1-6H
InChi Key WDJLPQCBTBZTRH-UHFFFAOYSA-N
Smiles C1=CC=C2C(=C1)C(=CS2)C=O
Isomeric SMILES C1=CC=C2C(=C1)C(=CS2)C=O
分子量 162.21
Reaxy-Rn 114116
Reaxys-RN link address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=114116&ln=

化学和物理性质

敏感性 对空气敏感
闪点(℉) >235.4 °F
闪点(℃) >113 °C
沸点 133 °C/4 mmHg
熔点 53-57°C
分子量 162.210 g/mol
XLogP3 2.600
氢键供体数Hydrogen Bond Donor Count 0
氢键受体数Hydrogen Bond Acceptor Count 2
可旋转键计数Rotatable Bond Count 1
精确质量Exact Mass 162.014 Da
单同位素质量Monoisotopic Mass 162.014 Da
拓扑极表面积Topological Polar Surface Area 45.300 Ų
重原子数Heavy Atom Count 11
形式电荷Formal Charge 0
复杂度Complexity 158.000
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
WGK Germany 3
个人防护装备 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter

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找到9个结果

批号(Lot Number) 证书类型 货号
H2527055 分析证书 B152938
L2206572 分析证书 B152938
L2206573 分析证书 B152938
L2206591 分析证书 B152938
K2101033 分析证书 B152938
J2130382 分析证书 B152938
J2130381 分析证书 B152938
G2031039 分析证书 B152938
G2031038 分析证书 B152938

此产品的引用文献

引用文献

1. Linlin Sun, Xiaoshuo Liu, Huiling Ji, Xunlei Ding, Nan Jiang, Jigang Wang.  (2023)  Novel electron donor boosting the electron supply capacity of hierarchical structure carbon nitride for efficient photocatalytic hydrogen peroxide production.  CHEMICAL ENGINEERING JOURNAL,  474  (145468).  [10.1016/j.cej.2023.145468]

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