产品名称
苯并噻唑-6-羧酸, 96%
InChI
1S/C8H5NO2S/c10-8(11)5-1-2-6-7(3-5)12-4-9-6/h1-4H,(H,10,11)
SMILES string
OC(=O)c1ccc2ncsc2c1
InChI key
DMPZJACLHDWUFS-UHFFFAOYSA-N
assay
96%
mp
245-251 °C (lit.)
functional group
carboxylic acid
Quality Level
Application
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。
General description
苯并噻唑-6-羧酸 (BTCA) 是苯并噻唑衍生物。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
James W. Noah et al.
Probe Reports from the NIH Molecular Libraries Program, 2012 Dec 17 (Updated 2013 Apr 5) (2013-07-09)
Uropathogenic
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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