2-Amino-6-bromobenzothiazole

Modify Date: 2025-08-25 12:42:20

2-Amino-6-bromobenzothiazole Structure
2-Amino-6-bromobenzothiazole structure
Common Name 2-Amino-6-bromobenzothiazole
CAS Number 15864-32-1 Molecular Weight 229.10
Density 1.8±0.1 g/cm3 Boiling Point 366.8±34.0 °C at 760 mmHg
Molecular Formula C7H5BrN2S Melting Point 213-217 °C(lit.)
MSDS Chinese USA Flash Point 175.7±25.7 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 2-Amino-6-bromobenzothiazole


2-Amino-6-bromobenzothiazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 2-Amino-6-bromobenzothiazole
Synonym More Synonyms

 2-Amino-6-bromobenzothiazole Biological Activity

Description 2-Amino-6-bromobenzothiazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.8±0.1 g/cm3
Boiling Point 366.8±34.0 °C at 760 mmHg
Melting Point 213-217 °C(lit.)
Molecular Formula C7H5BrN2S
Molecular Weight 229.10
Flash Point 175.7±25.7 °C
Exact Mass 227.935669
PSA 67.15000
LogP 2.66
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.783
Storage condition Room temperature.

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302-H317-H319
Precautionary Statements P280-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard Codes Xn:Harmful;
Risk Phrases R22;R36;R43
Safety Phrases S26-S36/37
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2934999090

 Synthetic Route

 Customs

HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles4

More Articles
Prokaryotic NavMs channel as a structural and functional model for eukaryotic sodium channel antagonism.

Proc. Natl. Acad. Sci. U. S. A. 111(23) , 8428-33, (2014)

Voltage-gated sodium channels are important targets for the development of pharmaceutical drugs, because mutations in different human sodium channel isoforms have causal relationships with a range of ...

Efficient synthesis of 2-amino-6-arylbenzothiazoles via Pd (0) Suzuki cross coupling reactions: potent urease enzyme inhibition and nitric oxide scavenging activities of the products. Gull Y, et al.

Molecules 18(8) , 8845-8857, (2013)

Synthesis, cytostatic, and antitumor properties of new Rh (I) thiazole complexes. Craciunescu, D. G., et al.

Biol. Trace Elem. Res. 8(4) , 251-261, (1985)

 Synonyms

2-Amino-6-bromobenzothiazole
MFCD00152229
2-Amino-6-Bromo benthiazole
6-Bromobenzo[d]thiazol-2-amine
2-Benzothiazolamine, 6-bromo-
6-Bromo-1,3-benzothiazol-2-amine
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