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1-ACETYLINDOLINE

1-ACETYLINDOLINE Struktur
16078-30-1
CAS-Nr.
16078-30-1
Englisch Name:
1-ACETYLINDOLINE
Synonyma:
1-ACETYLINDOLINE;1-acetyl-indolin;N-ACETYL INDOLINE;Acetylindoline,N-;1-ACETYLINDOLINE 98+%;1-ACETYL-2,3-DIHYDROINDOLE;1-acetyl-2,3-dihydro-1h-indol;1-Acetyl-2,3-dihydro-1H-indole;1H-Indole, 1-acetyl-2,3-dihydro-;1-(2,3-DIHYDRO-INDOL-1-YL)-ETHANONE
CBNumber:
CB5487514
Summenformel:
C10H11NO
Molgewicht:
161.2
MOL-Datei:
16078-30-1.mol
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1-ACETYLINDOLINE Eigenschaften

Schmelzpunkt:
102-104 °C(lit.)
Siedepunkt:
125-130 °C(Press: 1 Torr)
Dichte
1.144±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
1.13±0.20(Predicted)
CAS Datenbank
16078-30-1(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
S-Sätze: 22-24/25
WGK Germany  3
RTECS-Nr. NM1892500
HS Code  2933998090
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

1-ACETYLINDOLINE Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Verwenden

• ;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

Allgemeine Beschreibung

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.

1-ACETYLINDOLINE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

methyl indoline-5-carboxylate 5-Brom-7-nitroindolin 5-BROMOINDOLINE 5-Acetylindole 1-acetylindoline-5-carbonitrile 1-(7-Bromoindolin-1-yl)ethanone 1H-Indole,7-ethoxy-2,3-dihydro-(9CI) Ethanone, 1-(1-acetyl-2,3-dihydro-1H-indol-5-yl)-2-[bis(phenylMethyl)aMino]- 1-ACETYL-7-BROMOINDOLIN-5-AMINE 1 5-DIACETYLINDOLINE 97

1-ACETYLINDOLINE Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 199)Lieferanten
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sales@alchempharmtech.com United States 63711 58
SIMAGCHEM CORP 		+86-13806087780
 sale@simagchem.com China 17367 58
Career Henan Chemica Co 		+86-0371-86658258 15093356674;
 laboratory@coreychem.com China 30255 58

16078-30-1()Verwandte Suche:

1-Acetyl-1H-indol-3-carbaldehyd Indolin Strychnin Brucin Brucinsulfat Strychnidin-10-on-sulfat (2:1) 1-Acetyl-1H-indol-2,3-dion Strychnidin-10-onmononitrat Strychninhydrochlorid 1-Acetyl-5-nitroindolin Strychnidin-10-on, 19-Oxid 1-(2,3-Dihydro-1H-indol-5-yl)ethan-1-on
  • 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)-
  • 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
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