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Merck
CN

489689

Sigma-Aldrich

3-甲基-5-异噁唑乙酸

98%

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About This Item

经验公式(希尔记法):
C6H7NO3
CAS号:
分子量:
141.12
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

98%

mp

101-104 °C (lit.)

官能团

carboxylic acid

SMILES字符串

Cc1cc(CC(O)=O)on1

InChI

1S/C6H7NO3/c1-4-2-5(10-7-4)3-6(8)9/h2H,3H2,1H3,(H,8,9)

InChI key

POEFJFLAFQWOTL-UHFFFAOYSA-N

一般描述

3-Methyl-5-isoxazoleacetic acid is a substituted isoxazole.

应用

3-Methyl-5-isoxazoleacetic acid may be used as a reagent in the solid phase synthesis of von Hippel-Lindau protein (VHL) ligands. It may also be used to prepare (N-(4-chlorophenyl)-α-[[(4-chlorophenyl)amino]methylene]-3-methyl-5-isoxazoleacetamide).

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The Journal of pharmacology and experimental therapeutics, 336(3), 908-915 (2010-12-17)
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Dennis L Buckley et al.
Journal of the American Chemical Society, 134(10), 4465-4468 (2012-03-01)
E3 ubiquitin ligases, which bind protein targets, leading to their ubiquitination and subsequent degradation, are attractive drug targets due to their exquisite substrate specificity. However, the development of small-molecule inhibitors has proven extraordinarily challenging as modulation of E3 ligase activities

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