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2-AMINO-4-CHLOROBENZOTHIAZOLE

2-AMINO-4-CHLOROBENZOTHIAZOLE Basic information
Product Name:2-AMINO-4-CHLOROBENZOTHIAZOLE
Synonyms:2-amino-4-chloro-benzothiazol;TIMTEC-BB SBB000250;4-CHLORO-1,3-BENZOTHIAZOL-2-AMINE;AKOS BB-8273;2-AMINO-4-CHLOROBENZOTHIAZOLE;4-chlorobenzothiazol-2-ylamine;2-Benzothiazolamine,4-chloro-(9CI);LABOTEST-BB LT00012587
CAS:19952-47-7
MF:C7H5ClN2S
MW:184.65
EINECS:243-439-5
Product Categories:Building Blocks;Halogenated Heterocycles;BENZOTHIAZOLE;Thiazoles;Heterocyclic Building Blocks;ThiazolesHeterocyclic Building Blocks
Mol File:19952-47-7.mol
2-AMINO-4-CHLOROBENZOTHIAZOLE Structure
2-AMINO-4-CHLOROBENZOTHIAZOLE Chemical Properties
Melting point 203-205 °C (lit.)
Boiling point 344.3±34.0 °C(Predicted)
density 1.4750 (rough estimate)
refractive index 1.6100 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka2.14±0.10(Predicted)
form Crystalline Powder
color White to light beige or grayish
BRN 136784
InChIKeyOEQQFQXMCPMEIH-UHFFFAOYSA-N
CAS DataBase Reference19952-47-7(CAS DataBase Reference)
EPA Substance Registry System2-Amino-4-chlorobenzothiazole (19952-47-7)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 26-37/39-36
WGK Germany 2
RTECS DL1225000
TSCA Yes
HS Code 29342080
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
2-AMINO-4-CHLOROBENZOTHIAZOLE Usage And Synthesis
Chemical Propertieswhite to light beige or greyish crystalline powder
Uses2-Amino-4-chlorobenzothiazole is a benzothiazole derivative that shows in vivo antiviral effects against various influenza A2 strains.
General DescriptionCream colored crystalline solid.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileA halogenated amine, organosulfide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
Health HazardACUTE/CHRONIC HAZARDS: When heated to decomposition 2-AMINO-4-CHLOROBENZOTHIAZOLE emits very toxic fumes of chloride ion, SOx and NOx.
Fire HazardFlash point data for 2-AMINO-4-CHLOROBENZOTHIAZOLE are not available; however, 2-AMINO-4-CHLOROBENZOTHIAZOLE is probably combustible.
2-AMINO-4-CHLOROBENZOTHIAZOLE Preparation Products And Raw materials
Raw materials1-(2-Chlorophenyl)-2-thiourea
Preparation ProductsBenazolin-->4-Choro-2(3H)-benzothiazolone-->2(3H)-Benzothiazolone,4-chloro-,hydrazone(9CI)
SALOR-INT L117668-1EA 1-(4-CHLORO-2-BENZOTHIAZOLYL)-3-METHYL UREA Benzothiazole 2-Amino-4,6-dichlorobenzothiazole SALOR-INT L117633-1EA methyl [(4-chloro-1,3-benzothiazol-2-yl)amino](oxo)acetate 2-Benzothiazolamine,4-chloro-6-methyl-(9CI) SALOR-INT L117641-1EA 2-AMINO-4-CHLOROBENZOTHIAZOLE HYDROBROMIDE SALOR-INT L117595-1EA 2-AMINO-4-CHLOROBENZOTHIAZOLE 6-BROMO-4-CHLORO-1,3-BENZOTHIAZOL-2-AMINE SALOR-INT L117617-1EA SALOR-INT L117625-1EA SALOR-INT L117609-1EA N-(4-CHLOROBENZO[D]THIAZOL-2-YL)CYCLOPROPANECARBOXAMIDE 2-Amino-4,5-dichlorobenzothiazole. Benzothiazole, 4-chloro- (7CI,8CI,9CI)
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