530336
Benzothiazole-6-carboxylic acid
96%
Sinónimos:
1,3-Benzothiazole-6-carboxylic acid, Benzo[d]thiazole-6-carboxylic acid
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About This Item
Fórmula empírica (notación de Hill):
C8H5NO2S
Número de CAS:
Peso molecular:
179.20
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
96%
mp
245-251 °C (lit.)
functional group
carboxylic acid
SMILES string
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
General description
Benzothiazole-6-carboxylic acid (BTCA) is a benzothiazole derivative.
Application
Benzothiazole-6-carboxylic acid may be used in the synthesis of N-(pyridin-4-yl)benzo[d]thiazole-6-carboxamide, which shows the potential to inhibit K1 capsule formation in uropathogenic Escherichia coli. It may also be used as an internal standard during the quantification of benzothiazoles by liquid chromatography-electrospray ionization-tandem mass spectrometry.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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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