CAS 16078-30-1|1-Acetylindoline

Introduction:Basic information about CAS 16078-30-1|1-Acetylindoline, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name1-Acetylindoline
CAS Number16078-30-1Molecular Weight161.200
Density1.1±0.1 g/cm3Boiling Point355.1±21.0 °C at 760 mmHg
Molecular FormulaC10H11NOMelting Point102-104 °C(lit.)
MSDSChineseUSAFlash Point174.5±13.3 °C

Names

Name1-Acetylindoline
SynonymMore Synonyms

Chemical & Physical Properties

Density1.1±0.1 g/cm3
Boiling Point355.1±21.0 °C at 760 mmHg
Melting Point102-104 °C(lit.)
Molecular FormulaC10H11NO
Molecular Weight161.200
Flash Point174.5±13.3 °C
Exact Mass161.084061
PSA20.31000
LogP1.76
Vapour Pressure0.0±0.8 mmHg at 25°C
Index of Refraction1.576
InChIKeyRNTCWULFNYNFGI-UHFFFAOYSA-N
SMILESCC(=O)N1CCc2ccccc21

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NM1892500
CHEMICAL NAME :
Indoline, 1-acetyl-
CAS REGISTRY NUMBER :
16078-30-1
BEILSTEIN REFERENCE NO. :
0129366
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C10-H11-N-O
MOLECULAR WEIGHT :
161.22
WISWESSER LINE NOTATION :
T56 BNT&J BV1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
204 mg/kg
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold
REFERENCE :
JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 20,1448,1977

Safety Information

Hazard CodesXn
Safety PhrasesS22-S24/25
RIDADRNONH for all modes of transport
WGK Germany3
RTECSNM1892500
HS Code2933990090

Customs

HS Code2933990090
Summary2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles3

More Articles
The synthesis of 5-and 7-acetylindole derivatives. I: The photochemical rearrangement of 1-acetylindoline. Akagi M and Ozaki K.

Heterocycles 26(!) , 61-64, (1987)

Highly Convenient and Large Scale Synthesis of 5-chloroindole and its 3-substituted Analogues Keetha L, et al.

J. Korean Chem. Soc. 55(2) , (2011)

Reduction of amides with silanes catalyzed by MoO2Cl2. Fernandes AC and Romão CC.

J. Mol. Catal. A: Chem. 272(1) , 60-63., (2007)

Synonyms

N-Acetylindoline
1-(Indolin-1-yl)ethanone
1-(2,3-Dihydro-1H-indol-1-yl)ethanone
1-(2,3-dihydroindol-1-yl)ethanone
Ethanone, 1-(2,3-dihydro-1H-indol-1-yl)-
MFCD00022908
N-Acetyl indoline
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