2-Bromothiazole

Modify Date: 2024-01-02 19:30:34

2-Bromothiazole Structure
2-Bromothiazole structure
Common Name 2-Bromothiazole
CAS Number 3034-53-5 Molecular Weight 164.02
Density 1.9±0.1 g/cm3 Boiling Point 171.0±9.0 °C at 760 mmHg
Molecular Formula C3H2BrNS Melting Point 171ºC
MSDS Chinese USA Flash Point 63.3±0.0 °C

 Use of 2-Bromothiazole


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

 Names

Name 2-bromo-1,3-thiazole
Synonym More Synonyms

 2-Bromothiazole Biological Activity

Description 2-Bromothiazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
In Vitro 2-溴噻唑,仅供研究使用。它也用作芳基卤化物,用于 N-芳基化 5-和 7-氮杂吲哚。铜催化氰化提供 2-氰基噻唑

 Chemical & Physical Properties

Density 1.9±0.1 g/cm3
Boiling Point 171.0±9.0 °C at 760 mmHg
Melting Point 171ºC
Molecular Formula C3H2BrNS
Molecular Weight 164.02
Flash Point 63.3±0.0 °C
Exact Mass 162.909119
PSA 41.13000
LogP 1.93
Vapour Pressure 1.9±0.3 mmHg at 25°C
Index of Refraction 1.605
Storage condition 2-8°C
Water Solubility insoluble

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)
Hazard Codes Xi: Irritant;F: Flammable;
Risk Phrases R36/37/38
Safety Phrases S23-S24/25
RIDADR 1993
WGK Germany 3
HS Code 29341000

 Customs

HS Code 2934100090
Summary 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 Articles5

More Articles
Synthesis and characterization of fused pyrrolo[3,2-d:4,5-d']bisthiazole-containing polymers.

Org. Lett. 12(23) , 5478-81, (2010)

The synthesis of a novel electron-deficient fused pyrrolo[3,2-d:4,5-d']bisthiazole is reported from 2-bromothiazole. This was copolymerized with thiophene, selenophene, thienothiophene, and bithiophen...

Regioselective functionalization of the thiazole scaffold using TMPMgCl·LiCl and TMP2Zn·2MgCl2·2LiCl.

J. Org. Chem. 76(16) , 6972-8, (2011)

A general method for the synthesis of 2,4,5-trisubstituted thiazoles has been developed. Starting from commercially available 2-bromothiazole, successive metalations using TMPMgCl·LiCl or TMP(2)Zn·2Mg...

Tetrahedron Lett. 48 , 4831, (2007)

 Synonyms

2-Bromothiazole
2-bromo-thiazole
2-Bromo-1,3-thiazole
bromothiazole
MFCD00005316
2-Bromo thiazole
EINECS 221-229-4
2-Thiazolyl Bromide
2-bromothioazole
Thiazole, 2-bromo-
Thiazole,2-bromo
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