CAS 3034-53-5|2-Bromothiazole

Introduction:Basic information about CAS 3034-53-5|2-Bromothiazole, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name2-Bromothiazole
CAS Number3034-53-5Molecular Weight164.02
Density1.9±0.1 g/cm3Boiling Point171.0±9.0 °C at 760 mmHg
Molecular FormulaC3H2BrNSMelting Point171ºC
MSDSChineseUSAFlash Point63.3±0.0 °C

Names

Name2-bromo-1,3-thiazole
SynonymMore Synonyms

2-Bromothiazole BiologicalActivity

Description2-Bromothiazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related CatalogResearch Areas >>Others
In Vitro2-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

Density1.9±0.1 g/cm3
Boiling Point171.0±9.0 °C at 760 mmHg
Melting Point171ºC
Molecular FormulaC3H2BrNS
Molecular Weight164.02
Flash Point63.3±0.0 °C
Exact Mass162.909119
PSA41.13000
LogP1.93
Vapour Pressure1.9±0.3 mmHg at 25°C
Index of Refraction1.605
InChIKeyRXNZFHIEDZEUQM-UHFFFAOYSA-N
SMILESBrc1nccs1
Storage condition2-8°C
Water Solubilityinsoluble

Safety Information

Personal Protective EquipmentEyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)
Hazard CodesXi: Irritant;F: Flammable;
Risk PhrasesR36/37/38
Safety PhrasesS23-S24/25
RIDADR1993
WGK Germany3
HS Code29341000

Customs

HS Code2934100090
Summary2934100090 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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