产品名称

英文名称：1-Acetylindoline

同义词

1-Acetylindoline、16078-30-1、1-(indolin-1-yl)ethanone、N-Acetylindoline、1-(2,3-dihydroindol-1-yl)ethanone、1H-Indole, 1-acetyl-2,3-dihydro-、1-(2,3-dihydro-1H-indol-1-yl)ethan-1-one、MFCD00022908、CHEMBL3274978、1-(2,3-dihydro-indol-1-yl)-ethanone、Ethanone, 1-(2、1-乙酰基吲哚啉

产品性质

CAS编号：16078-30-1

分子式：C10H11NO

分子量：161.2

MDL号：MFCD00022908

PubChem编号：27673

别名：1-乙酰基吲哚啉

英文别名：1-Acetylindoline|16078-30-1|1-(indolin-1-yl)ethanone|N-Acetylindoline|1-(2,3-dihydroindol-1-yl)ethanone|1H-Indole, 1-acetyl-2,3-dihydro-|1-(2,3-dihydro-1H-indol-1-yl)ethan-1-one|MFCD00022908|CHEMBL3274978|1-(2,3-dihydro-indol-1-yl)-ethanone|Ethanone, 1-(2

规格或纯度：98%

英文名称：1-Acetylindoline

运输条件：常规运输

产品介绍：It is a tertiary amide having bulky N-groups. Its reduction to the corresponding amine, by reaction with silane in the presence of MoO2Cl2 (catalyst), has been reported.. Reactant for preparation of triazolothiadiazepine dioxide derivatives . Reactant for preparation of halo-substituted aromatic amides . Reactant for preparation of [[(phenyl)piperazinyl]alkyl]indolyl]ethanone and [[[(phenoxyethyl)piperazinyl]alkyl]indolyl]ethanone derivatives as α1-adrenoreceptor antagonists . Reactant for synthesis of naphthalenedione derivatives as antimycobacterial agents . Reactant for regioselective ortho Suzuki-Miyaura coupling reaction It may be used in the synthesis of 5-chloroindole.

PubChem SID：488183055

PubChem SID url：https//pubchem.ncbi.nlm.nih.gov/substance/488183055

IUPAC Name：1-(2,3-dihydroindol-1-yl)ethanone

INCHI：InChI=1S/C10H11NO/c1-8(12)11-7-6-9-4-2-3-5-10(9)11/h2-5H,6-7H2,1H3

InChi Key：RNTCWULFNYNFGI-UHFFFAOYSA-N

Canonical SMILES：CC(=O)N1CCC2=CC=CC=C21

Isomeric SMILES：CC(=O)N1CCC2=CC=CC=C21

WGK Germany：3

RTECS：NM1892500

PubChem CID：27673

熔点：102-104°C

产品包装