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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:
Assay:
97%
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。
signalword
Danger
hcodes
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
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)
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)
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)
Viktoras Dryza et al.
The journal of physical chemistry. A, 116(17), 4323-4329 (2012-04-14)
Electronic spectra of the gas-phase isoquinoline(+)-Ar and quinoline(+)-Ar complexes are recorded using photodissociation spectroscopy by monitoring the Ar loss channel. The D(3)←D(0) and D(4)←D(0) band origins for isoquinoline(+)-Ar are observed at 15245 ± 15 cm(-1) and 21960 ± 15 cm(-1)
Vikas Tyagi et al.
Organic letters, 14(12), 3126-3129 (2012-05-26)
A novel ligand-free palladium-catalyzed cascade reaction for the synthesis of highly diverse isoquinolin-1(2H)-one derivatives from isocyanide and amide precursors synthesized by Ugi-MCR has been developed. A broad variety of acids, amines, and isocyanides were used as starting materials for Ugi-MCR
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