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N-已酰基吲哚啉

N-已酰基吲哚啉名称

[ CAS 号 ]:
16078-30-1

[ 中文名 ]:
N-乙酰基吲哚啉

[ 英文名 ]:
1-Acetylindoline

[中文别名 ]:

[英文别名 ]:

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

N-已酰基吲哚啉物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
355.1±21.0 °C at 760 mmHg

[ 熔点 ]:
102-104 °C(lit.)

[ 分子式 ]:
C₁₀H₁₁NO

[ 分子量 ]:
161.200

[ 闪点 ]:
174.5±13.3 °C

[ 精确质量 ]:
161.084061

[ PSA ]:
20.31000

[ LogP ]:
1.76

[ 外观性状 ]:
灰白色晶体

[ 蒸汽压 ]:
0.0±0.8 mmHg at 25°C

[ 折射率 ]:
1.576

[ 储存条件 ]:
室温

N-已酰基吲哚啉MSDS

详细MSDS(安全技术说明书)

N-已酰基吲哚啉毒性和生态

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

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N-已酰基吲哚啉安全信息

[ 危害码 (欧洲) ]:
Xn

[ 安全声明 (欧洲) ]:
S22-S24/25

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ RTECS号 ]:
NM1892500

[ 海关编码 ]:
2933990090

N-已酰基吲哚啉合成路线

详细合成路线

N-已酰基吲哚啉上下游产品

N-已酰基吲哚啉上游产品

N-已酰基吲哚啉下游产品

N-已酰基吲哚啉海关

[ 海关编码 ]: 2933990090

[ 中文概述 ]:
2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

N-已酰基吲哚啉文献

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)

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