663190
5-甲基吲哚-2-羧酸乙酯
97%
别名:
5-Methylindole-2-carboxylic acid ethyl ester, NSC 30928
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关于此项目
经验公式（希尔记法）:
C12H13NO2
化学文摘社编号:
分子量:
203.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
5-甲基吲哚-2-羧酸乙酯, 97%
InChI
1S/C12H13NO2/c1-3-15-12(14)11-7-9-6-8(2)4-5-10(9)13-11/h4-7,13H,3H2,1-2H3
SMILES string
CCOC(=O)c1cc2cc(C)ccc2[nH]1
InChI key
KMVFKXFOPNKHEM-UHFFFAOYSA-N
assay
97%
form
solid
mp
160-164 °C
functional group
ester
Quality Level
Application
- Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions
- Reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists
- Reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents
- Reactant for Friedel-Crafts acylation with nitrobenzoyl chloride
- Reactant for oximation reactions
General description
Ethyl 5-methylindole-2-carboxylate (5-Methylindole-2-carboxylic acid ethyl ester) is an indole derivative. Indole ring system is an important building block or intermediate in the synthesis of many pharmaceutical agents. It is formed during the Fischer indolization of ethyl pyruvate 2-[2-(methanesulfonyloxy)-4-methyl]phenylhydrazine.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Substituent Effects in the Fischer Indolization of (2-Sulfonyloxyphenyl) hydrazones (Fischer Indolization and Related Compounds. XXX).
Murakami Y, et al.
Chemical & Pharmaceutical Bulletin, 47, 791-797 (1999)
商品
Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
傅-克酰基化反应是一种芳烃与酰氯或酸酐使用强路易斯酸催化剂的反应。该反应通过亲电芳族取代进行，形成单酰化产物。
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