产品名称

英文名称：Ethyl 5-methylindole-2-carboxylate

同义词

Ethyl 5-methylindole-2-carboxylate、16382-15-3、ethyl 5-methyl-1H-indole-2-carboxylate、2-CARBETHOXY-5-METHYLINDOLE、MFCD00022703、1H-Indole-2-carboxylic acid, 5-methyl-, ethyl ester、NSC30928、5-Methylindole-2-carboxylic acid ethyl ester、5-methyl-1H-indole-2-ca、5-甲基吲哚-2-羧酸乙酯

产品性质

CAS编号：16382-15-3

分子式：C12H13NO2

分子量：203.24

MDL号：MFCD00022703

PubChem编号：232919

别名：5-甲基吲哚-2-羧酸乙酯

英文别名：Ethyl 5-methylindole-2-carboxylate|16382-15-3|ethyl 5-methyl-1H-indole-2-carboxylate|2-CARBETHOXY-5-METHYLINDOLE|MFCD00022703|1H-Indole-2-carboxylic acid, 5-methyl-, ethyl ester|NSC30928|5-Methylindole-2-carboxylic acid ethyl ester|5-methyl-1H-indole-2-ca

规格或纯度：99%

英文名称：Ethyl 5-methylindole-2-carboxylate

应用：A compound for the synthesis of biological active chemicals.

运输条件：常规运输

备注：1g卖完停产，不再备货

产品介绍：It 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.A compound for the synthesis of biological active chemicals.It 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.A compound for the synthesis of biological active chemicals.

PubChem SID：488188840

IUPAC Name：ethyl 5-methyl-1H-indole-2-carboxylate

INCHI：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

InChi Key：KMVFKXFOPNKHEM-UHFFFAOYSA-N

Canonical SMILES：CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C

Isomeric SMILES：CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C

WGK Germany：3

PubChem CID：232919

溶解性：Soluble in methanol, and dichloromethane. Insoluble in water.

沸点：236°C/4mm

熔点：160-164 °C

个人防护装备：Eyeshields， Gloves， type N95 (US)， type P1 (EN143) respirator filter

产品包装