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Merck
CN
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文件

515205

Sigma-Aldrich

吲哚-3-乙醛酰氯

98%

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别名:
α-Oxoindole-3-acetyl chloride, 2-(3-Indolyl)-2-oxoacetyl chloride, NSC 128332
经验公式（希尔记法）:
C10H6ClNO2
CAS号:
22980-09-2
分子量:
207.61
EC 号:
245-362-2
MDL编号:
MFCD00015460
UNSPSC代码:
12352100
PubChem化学物质编号:
24873804
NACRES:
NA.22

检测方案

98%

mp

138 °C (dec.) (lit.)

储存温度

2-8°C

SMILES字符串

ClC(=O)C(=O)c1c[nH]c2ccccc12

InChI

1S/C10H6ClNO2/c11-10(14)9(13)7-5-12-8-4-2-1-3-6(7)8/h1-5,12H

InChI key

FPEGGKCNMYDNMW-UHFFFAOYSA-N

应用

  • Reactant for preparation of dual IGF-1R/SRC inhibitors
  • Reactant for preparation of indolylglyoxylamides as a new class of antileishmanial agents
  • Reactant for preparation of glyoxyl analogs of indole phytoalexins as anticancer agents
  • Reactant for diastereoselective synthesis of heptacyclic core of dragmacidin E
  • Reactant for preparation of benzoylmethylpyrrolopyridinylethanedione as HIV-1 inhibitor
  • Reactant for preparation of fascaplysin-inspired diindolyls as selective inhibitors of CDK4/cyclin D1

象形图

Corrosion
GHS05

警示用语：

Danger

危险声明

H314

危险分类

Skin Corr. 1B

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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A concise synthesis of an AHR endogenous ligand with the indolecarbonylthiazole skeleton.
Grzywacz P, et al.
Heterocycles, 60(5), 1219-1224 (2003)
Notes-Concerning a preparation of tryptamine.
Brutcher J, et al.
The Journal of Organic Chemistry, 23(1), 146-147 (1958)
Manabu Nakazono et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 19(1), 123-127 (2003-02-01)
The chemiluminescence (CL) intensities of various indole derivatives substituted with a glyoxylyl group at the 3-position and a hydroxyl group at the 5-position of the indole ring were compared upon the addition of H2O2 in alkaline media. The CL intensities

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