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Merck
CN

549304

Sigma-Aldrich

4′-(甲磺酰)苯乙酮

97%

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别名:
4-(甲磺酰)苯乙酮
线性分子式:
CH3SO2C6H4COCH3
CAS号:
分子量:
198.24
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

检测方案

97%

mp

126-129 °C (lit.)

SMILES字符串

CC(=O)c1ccc(cc1)S(C)(=O)=O

InChI

1S/C9H10O3S/c1-7(10)8-3-5-9(6-4-8)13(2,11)12/h3-6H,1-2H3

InChI key

KAVZYDHKJNABPC-UHFFFAOYSA-N

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应用

4′-(Methylsulfonyl)acetophenone may be used in the synthesis of:
  • 3-(4-Methylsulfonylphenyl)-4-phenyl-2(5H)-furanone with potent apoptosis-inducing ability.
  • Bromo-4-methylsulfonylacetophenone, an intermediate for preparing DL-threo-2-dichloroacetamido-1-(4-methylsulfonylphenyl)-1,3-propanediol.
  • 1-N-Substituted-3,5-diphenyl-2-pyrazoline derivatives, which show promising anti-inflammatory activity.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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New Antibacterial Agents. II. An Alternate Synthesis of DL-threo-2-Dichloro-acetamido-1-(4-methylsulfonylphenyl)-1, 3-propanediol1.
Suter CM, et al.
Journal of the American Chemical Society, 75(17), 4330-4333 (1953)
Rossella Fioravanti et al.
European journal of medicinal chemistry, 45(12), 6135-6138 (2010-10-27)
Eighteen new 1-N-substituted-3,5-diphenyl-2-pyrazoline derivatives have been synthesized and cyclooxygenase (COX-1 and COX-2) inhibitory activities have been evaluated. The results of these biological assays showed that all of new derivatives are not endowed with improved anti-inflammatory activity against COX-1, but some
Jiuxiang Zhu et al.
Journal of the National Cancer Institute, 94(23), 1745-1757 (2002-12-05)
The cyclooxygenase-2 (COX-2) inhibitor celecoxib is thought to act as a chemopreventive agent by sensitizing cancer cells to apoptotic signals. Other COX-2 inhibitors, such as rofecoxib, are two orders of magnitude less potent than celecoxib at inducing apoptosis. The molecular

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