1-ACETYLINDOLINE

1-ACETYLINDOLINE Structure
CAS No.
16078-30-1
Chemical Name:
1-ACETYLINDOLINE
Synonyms
1-ACETYLINDOLINE;1-acetyl-indolin;N-ACETYL INDOLINE;Acetylindoline,N-;1-ACETYLINDOLINE 98+%;1-ACETYL-2,3-DIHYDROINDOLE;1-(indolin-1-yl)ethan-1-one;1-acetyl-2,3-dihydro-1h-indol;1-Acetyl-2,3-dihydro-1H-indole;1H-Indole, 1-acetyl-2,3-dihydro-
CBNumber:
CB5487514
Molecular Formula:
C10H11NO
Molecular Weight:
161.2
MOL File:
16078-30-1.mol
Modify Date:
2022/12/30 16:20:48

1-ACETYLINDOLINE Properties

Melting point 102-104 °C(lit.)
Boiling point 125-130 °C(Press: 1 Torr)
Density 1.144±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka 1.13±0.20(Predicted)
CAS DataBase Reference 16078-30-1(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H317
Precautionary statements  P280
Safety Statements  22-24/25
WGK Germany  3
RTECS  NM1892500
HS Code  2933998090
NFPA 704
1
2 0

1-ACETYLINDOLINE price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 379492 1-Acetylindoline 98% 16078-30-1 5G ₹4384.13 2022-06-14 Buy
Product number Packaging Price Buy
379492 5G ₹4384.13 Buy

1-ACETYLINDOLINE Chemical Properties,Uses,Production

Uses

• ;Reactant for preparation of triazolothiadiazepine dioxide derivatives1• ;Reactant for preparation of halo-substituted aromatic amides2• ;Reactant for preparation of [[(phenyl)piperazinyl]alkyl]indolyl]ethanone and [[[(phenoxyethyl)piperazinyl]alkyl]indolyl]ethanone derivatives as α1-adrenoreceptor antagonists3• ;Reactant for synthesis of naphthalenedione derivatives as antimycobacterial agents4• ;Reactant for regioselective ortho Suzuki-Miyaura coupling reaction5

Synthesis Reference(s)

Tetrahedron, 52, p. 7525, 1996 DOI: 10.1016/0040-4020(96)00266-9
Tetrahedron Letters, 24, p. 561, 1983 DOI: 10.1016/S0040-4039(00)81464-1

General Description

1-Acetylindoline, a substituted indole, 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.

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1-acetyl-2,3-dihydro-1h-indol 1-acetyl-indolin 1-(2,3-DIHYDRO-1H-INDOL-1-YL)ETHAN-1-ONE 1-(2,3-DIHYDRO-INDOL-1-YL)-ETHANONE 1-ACETYL-2,3-DIHYDROINDOLE 1-ACETYLINDOLINE Acetylindoline,N- 1H-Indole, 1-acetyl-2,3-dihydro- (9CI) N-ACETYL INDOLINE 1-ACETYLINDOLINE 98+% 1H-Indole, 1-acetyl-2,3-dihydro- 1-Acetyl-2,3-dihydro-1H-indole Ethanone, 1-(2,3-dihydro-1H-indol-1-yl)- 1-(indolin-1-yl)ethan-1-one 16078-30-1 Indoles Heterocyclic Building Blocks Building Blocks Building Blocks C10 Chemical Synthesis Heterocyclic Building Blocks Building Blocks Heterocyclic Building Blocks Indoles Indoline & Oxindole ACETYLGROUP Indoles and derivatives