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QUINOLINE-2-CARBONITRILE

QUINOLINE-2-CARBONITRILE Structure
QUINOLINE-2-CARBONITRILE structure
CAS No.
1436-43-7
Chemical Name:
QUINOLINE-2-CARBONITRILE
Synonyms
Quinaldonitrile;2-Cyanoquinoline;Quinolinecarbonitrile;quinolin-2-carbonitrile;2-QUINOLINECARBONITRILE;QUINOLINE-2-CARBONITRILE;Quinoline-2-Carbinitrile;Quinoline-2-carbonitrile 97%;2-Quinolinecarbonitrile ,97%;QUINOLINE-2-CARBONITRILE ISO 9001：2015 REACH
CBNumber:
CB4396978
Molecular Formula:
C10H6N2
Molecular Weight:
154.17
MDL Number:
MFCD00134341
MOL File:
1436-43-7.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

QUINOLINE-2-CARBONITRILE Properties

Melting point 93-95 °C (lit.)
Boiling point 160°C 23mm
Density 1.21
refractive index 1.4820 (estimate)
Flash point 160°C/23mm
storage temp. Inert atmosphere,Room Temperature
pka -0.56±0.40(Predicted)
form powder to crystal
color White to Orange to Green
Water Solubility Insoluble in water.
BRN 115213

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352+P312-P304+P340+P312-P305+P351+P338
Hazard Codes  Xn,Xi
Risk Statements  20/21/22-36/37/38
Safety Statements  26-36
RIDADR  3439
WGK Germany  3
HazardClass  6.1
PackingGroup  III
HS Code  2933499090
NFPA 704
1
2 0

QUINOLINE-2-CARBONITRILE Chemical Properties,Uses,Production

Uses

Quinoline-2-carbonitrile is used to produce quinoline-2-carboxylic acid amide. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 4004, 1959 DOI: 10.1021/ja01524a046

General Description

Mechanism of the photoinduced substitution reaction of 2-quinolinecarbonitrile in alcohols or ethers has been reported. Photoinitiated dimerization of 2-quinolinecarbonitrile in HCl-acidified 2-propanol/water has been investigated at 77K and 331K. Benzophenone-sensitization of 2-quinolinecarbonitrile has been reported to yield triazapentaphene.

QUINOLINE-2-CARBONITRILE Preparation Products And Raw materials

Raw materials

Acetonitrile Quinoline Benzoyl chloride POTASSIUM CYANIDE

Preparation Products

2-Quinolinemethanamine Quinaldic acid N-methylquinolin-2-amine

QUINOLINE-2-CARBONITRILE Spectrum

QUINOLINE-2-CARBONITRILE(1436-43-7)1HNMRQUINOLINE-2-CARBONITRILE(1436-43-7)IRQUINOLINE-2-CARBONITRILE(1436-43-7)Raman

1436-43-7(QUINOLINE-2-CARBONITRILE)Related Search:

4-chloroquinoline-2-carbonitrile 8-HYDROXYQUINOLINE-2-CARBONITRILE QUINOLINE-2-CARBONITRILE 7,7,8,8-Tetracyanoquinodimethane ETHYL 4-CHLORO-8-CYANOQUINOXALINE-3-CARBOXYLATE
3-Cyanoquinoline 6-Fluoro-4-(trifluoromethyl)quinoline-2-carbonitrile ,97% 6-Cyanoquinoline 4-(Trifluoromethyl)quinoline-2-carbonitrile ,97% 2,3,5,6-Tetrafluoro-7,7,8,8-tetracyanoquinodimethane
2-Amino-4-methyl-quinoline-3-carbonitrile ,98% 11-OXO-2,3,6,7-TETRAHYDRO-1H,5H,11H-PYRANO[2,3-F]PYRIDO[3,2,1-IJ]QUINOLINE-10-CARBONITRILE 6-METHOXY-2-QUINOLINECARBONITR 2-CYANO-3-HYDROXYQUINOLINE 2-CYANO-3-BROMOQUINOLINE
6-BROMO-QUINOLINE-2-CARBONITRILE 2-CYANO-4-METHYLQUINOLINE 2-CYANO-3-METHYLQUINOLINE

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