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Merck
CN

219177

Sigma-Aldrich

4,5-二甲基噻唑

97%

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关于此项目

经验公式(希尔记法):
C5H7NS
化学文摘社编号:
分子量:
113.18
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案

97%

表单

powder

折射率

n20/D 1.521 (lit.)

沸点

158 °C/742 mmHg (lit.)

密度

1.07 g/mL at 25 °C (lit.)

SMILES字符串

Cc1ncsc1C

InChI

1S/C5H7NS/c1-4-5(2)7-3-6-4/h3H,1-2H3

InChI key

UWSONZCNXUSTKW-UHFFFAOYSA-N

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一般描述

Radical bromination of 4,5-dimethylthiazole using N-bromosuccinimide in the presence of 2,2′-azobisisobutyronitrile yields mono-, tri- and tetrabromo compounds.

应用

4,5-Dimethylthiazole was used in the preparation of 4-(bromomethyl)-5-(dibromomethyl)thiazole.

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

123.8 °F - closed cup

闪点(°C)

51 °C - closed cup

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mouaffak Al Hariri et al.
The Journal of organic chemistry, 62(2), 405-410 (1997-01-24)
4-(Bromomethyl)-5-(dibromomethyl)thiazole (1) was prepared in good yields by bromination of 4,5-dimethylthiazole with 3.3 equiv of NBS in the presence of AIBN. Treatment of 1 with sodium iodide led to a thiazole o-quinodimethane 2 which was trapped in situ with dienophiles
Selective Bromination of 4, 5-Dimethylthiazole with N-Bromosuccinimide.
Al Hariri M, et al.
European Journal of Organic Chemistry, 1998(4), 593-594 (1998)
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