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Merck
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주요 문서

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160474

Sigma-Aldrich

2-Bromothiazole

98%

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About This Item

실험식(Hill 표기법):
C3H2BrNS
CAS Number:
3034-53-5
Molecular Weight:
164.02
Beilstein:
105724
EC Number:
221-229-4
MDL number:
MFCD00005316
UNSPSC 코드:
12352100
PubChem Substance ID:
24849873
NACRES:
NA.22

분석

98%

양식

liquid

refractive index

n20/D 1.593 (lit.)

bp

171 °C (lit.)

density

1.82 g/mL at 25 °C (lit.)

작용기

bromo

저장 온도

2-8°C

SMILES string

Brc1nccs1

InChI

1S/C3H2BrNS/c4-3-5-1-2-6-3/h1-2H

InChI key

RXNZFHIEDZEUQM-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

2-Bromothiazole was used to N-arylate 5- and 7-azaindoles. 2-Bromothiazole was also used as starting reagent in the synthesis of:
  • 2-cyanothiazole via cpper-catalyzed cyanation
  • 2,4,5-trisubstituted thiazoles
  • novel electron-deficient fused pyrrolo[3,2-d:4,5-d′]bisthiazole
  • 3-(2′-thiazoyl)indoles

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point (°F)

closed cup - does not flash

Flash Point (°C)

closed cup - does not flash

개인 보호 장비

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
STBG8292
STBB8567V
STBB8687V
S39471
08210DE

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4-Methylthiazole 99%

Sigma-Aldrich

193925

4-Methylthiazole

5-Methylthiazole 97%

Sigma-Aldrich

302740

5-Methylthiazole

Cora Dunst et al.
The Journal of organic chemistry, 76(16), 6972-6978 (2011-07-09)
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·2MgCl(2)·2LiCl lead to the corresponding magnesated or zincated thiazoles which readily react with various electrophiles providing highly functionalized
Tetrahedron Letters, 48, 4831-4831 (2007)
Synlett, 555-555 (2007)
Mohammed Al-Hashimi et al.
Organic letters, 12(23), 5478-5481 (2010-11-12)
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 bithiophene by microwave-assisted Stille polycondensation. The resulting polymers exhibited small optical band gaps combined with low-lying HOMO energy levels and
Synthesis of camalexin and related phytoalexins.
Ayer WA, et al.
Tetrahedron, 48(14), 2919-2924 (1992)

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