![]() 2-Amino-6-bromobenzothiazole structure
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Common Name | 2-Amino-6-bromobenzothiazole | ||
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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 |
Signal Word | Warning |
Use of 2-Amino-6-bromobenzothiazole2-Amino-6-bromobenzothiazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 2-Amino-6-bromobenzothiazole |
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Synonym | More Synonyms |
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. |
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Related Catalog |
Density | 1.8±0.1 g/cm3 |
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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. |
Symbol |
![]() GHS07 |
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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 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2934999090 |
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Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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 ... |
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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)
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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)
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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 |