2-Amino-6-bromobenzothiazole

Names

[ Name ]:
2-Amino-6-bromobenzothiazole

[Synonym ]:
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

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]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

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.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

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

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

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%

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)