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About This Item
Empirical Formula (Hill Notation):
C9H7N
CAS Number:
Molecular Weight:
129.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-341-8
Beilstein/REAXYS Number:
107549
MDL number:
Assay:
97%
Quality Level
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.)
SMILES string
c1ccc2cnccc2c1
InChI
1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H
InChI key
AWJUIBRHMBBTKR-UHFFFAOYSA-N
Application
Isoquinoline can be used as:
- A catalyst in the synthesis of poly(imide)s.
- A reactant in the synthesis of N-benzyl isoquinoline-1,3,4-triones using iodine as a catalyst.
- A reactant in the synthesis of 2H-imidazo[5,1-a]isoquinolinium chloride.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
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
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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)
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)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| I28208-5G | 04061833327463 |
| I28208-100G | 04061833848715 |
| I28208-500G | 04061833848722 |
