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.
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1-Acetylindoline
Dangerous GoodsCAS number:16078-30-1 molecular formula:C10H11NO
overview
compound introduction
Specs
| Chinese alias | 1-乙酰基吲哚啉 | ||
| English alias | INDOLINE, 1-ACETYL- | F0451-0187 | 1-Acetylindoline, 98% | AKOS003239122 | HMS555O21 | SR-01000389835-1 | SB64066 | A-1414 | 1-(indolin-1-yl)ethan-1-one | RNTCWULFNYNFGI-UHFFFAOYSA-N | Maybridge1_005081 | 1-(2,3-dihydro-1H-indol-1-yl)ethan-1-one | 1-Acety | ||
| CAS number | 16078-30-1 | molecular formula | C10H11NO |
| molecular weight | 161.2 g/mol | Exact mass | ≥98% |
| PSA | 20.300 Ų | logp | 1.300 |
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Safety information
WGK Germany:
3
RTECS:
NM1892500
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