Merck
CN

219177

Sigma-Aldrich

4,5-二甲基噻唑

97%

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经验公式(希尔记法):
C5H7NS
CAS号:
分子量:
113.18
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

形式

powder

折射率

n20/D 1.521 (lit.)

bp

158 °C/742 mmHg (lit.)

密度

1.07 g/mL at 25 °C (lit.)

SMILES string

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.

法规信息

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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)
Le Wu et al.
Journal of molecular neuroscience : MN, 56(4), 848-857 (2015-02-24)
Lipoxin A4 (LXA4), a potent antioxidant and anti-inflammation mediator, protects brains against cerebral ischemia/reperfusion (I/R) injury in vivo. However, few reports concern its function on astrocytes during cerebral I/R injury. The pathogenesis of cerebral I/R injury involves oxidative stress caused
João G Marques et al.
Pharmaceutical research, 31(9), 2516-2528 (2014-03-14)
Cancer multi-drug resistance is a major issue associated with current anti-tumoral therapeutics. In this work, Crizotinib an anti-tumoral drug approved for the treatment of non-small lung cancer in humans, and Sildenafil (Viagra(®)), were loaded into micellar carriers to evaluate the
V Di Giacomo et al.
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Autophagy is a cellular defense mechanism which occurs through degradation and recycling of cytoplasmic constituents and represents a caspase—independent alternative to cell death by apoptosis. It is generally accepted that the suppression of autophagy in many cancer cells is directly

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