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Merck
CN

I28208

异喹啉

97%

别名:

β-喹啉, 2-氮杂萘, 2-苯并嗪, 苯并吡啶

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关于此项目

经验公式(希尔记法):
C9H7N
化学文摘社编号:
分子量:
129.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-341-8
Beilstein/REAXYS Number:
107549
MDL number:
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产品名称

异喹啉, 97%

InChI key

AWJUIBRHMBBTKR-UHFFFAOYSA-N

InChI

1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H

SMILES string

c1ccc2cnccc2c1

assay

97%

refractive index

n20/D 1.623 (lit.)

bp

242-243 °C (lit.)

mp

26-28 °C (lit.)

density

1.099 g/mL at 25 °C (lit.)

Quality Level

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Application

异喹啉可以用作:
  • 聚酰亚胺合成中的催化剂。
  • 通过碘作为催化剂合成 N-苄基异喹啉-1,3,4-三酮的反应物。
  • 合成2H-咪唑[5,1-a]异喹啉氯化物的反应物。

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Cascade Synthesis of Functionalized 2H-Imidazo [5, 1-a] isoquinolinium Chlorides from Isoquinoline, Chloroformamidines (= Carbamimidoyl Chlorides), and Isocyanides
Yavari I, et al.
Helvetica Chimica Acta, 93(1), 72-76 (2010)
Iodine-catalyzed oxidative multiple C-H bond functionalization of isoquinolines with methylarenes: an efficient synthesis of isoquinoline-1, 3, 4 (2 H)-triones
Zhu D, et al.
Organic & Biomolecular Chemistry, 15(34), 7112-7116 (2017)
Intrinsically microporous poly (imide) s: structure- porosity relationship studied by gas sorption and X-ray scattering
Ritter N, et al.
Macromolecules, 44(7), 2025-2033 (2011)
Jörg T Binder et al.
Journal of the American Chemical Society, 134(41), 17003-17006 (2012-10-09)
We have developed a nickel-catalyzed method for the asymmetric cross-coupling of secondary electrophiles with secondary nucleophiles, specifically, stereoconvergent Negishi reactions of racemic benzylic bromides with achiral cycloalkylzinc reagents. In contrast to most previous studies of enantioselective Negishi cross-couplings, tridentate pybox
Beta-phenylethylamines and the isoquinoline alkaloids.
K W Bentley
Natural product reports, 18(2), 148-170 (2001-05-05)

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