515205
吲哚-3-乙醛酰氯
98%
别名:
α-Oxoindole-3-acetyl chloride, 2-(3-Indolyl)-2-oxoacetyl chloride, NSC 128332
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关于此项目
经验公式（希尔记法）:
C10H6ClNO2
化学文摘社编号:
分子量:
207.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
245-362-2
MDL number:
产品名称
吲哚-3-乙醛酰氯, 98%
InChI key
FPEGGKCNMYDNMW-UHFFFAOYSA-N
InChI
1S/C10H6ClNO2/c11-10(14)9(13)7-5-12-8-4-2-1-3-6(7)8/h1-5,12H
SMILES string
ClC(=O)C(=O)c1c[nH]c2ccccc12
assay
98%
mp
138 °C (dec.) (lit.)
storage temp.
2-8°C
Application
- 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
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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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