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Merck
CN

530336

Sigma-Aldrich

苯并噻唑-6-羧酸

96%

别名:

1,3-苯并噻唑-6-羧酸, 苯并[d]噻唑-6-羧酸

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About This Item

经验公式(希尔记法):
C8H5NO2S
CAS号:
分子量:
179.20
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

96%

mp

245-251 °C (lit.)

官能团

carboxylic acid

SMILES字符串

OC(=O)c1ccc2ncsc2c1

InChI

1S/C8H5NO2S/c10-8(11)5-1-2-6-7(3-5)12-4-9-6/h1-4H,(H,10,11)

InChI key

DMPZJACLHDWUFS-UHFFFAOYSA-N

一般描述

苯并噻唑-6-羧酸 (BTCA) 是苯并噻唑衍生物。

应用

苯并噻唑-6-羧酸可用于合成N-(吡啶-4-基)苯并[d]噻唑-6-羧酰胺,表现出了抑制尿路致病性大肠杆菌中K1荚膜形成的潜力。在通过液相色谱-电喷雾电离串联质谱法定量苯并噻唑时,也可用其作内标。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

James W. Noah et al.
Probe Reports from the NIH Molecular Libraries Program, 2012 Dec 17 (Updated 2013 Apr 5) (2013-07-09)
Uropathogenic
Yoshihiro Sawada et al.
Pest management science, 59(1), 25-35 (2003-02-01)
The N'-benzoyl group of N-tert-butyl-N'-benzoyl-3,5-dimethylbenzohydrazide (1) was converted to a series of benzoheterocyclecarbonyl groups in order to investigate the potential usefulness of superimposing a hydrazine insecticide on 20-hydroxyecdysone. A series of analogues with benzodioxole, benzodioxane, benzodioxapine, indole, benzoxazole, benzoxazine or
Stefan Weiss et al.
Analytical chemistry, 77(22), 7415-7420 (2005-11-16)
The first method for the determination of commonly used corrosion inhibitors in environmental water samples by liquid chromatography-electrospray ionization-tandem mass spectrometry is presented. Benzotriazole (BTri) and the two isomers of tolyltriazole (5- and 4-TTri) are separated in an isocratic run.

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