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4-Methylpyridazine, 97%|580354|1120-88-3

4-Methylpyridazine, 97%

Cat. No JK580354_500_MG
J&K Chemical

Product Information

Product Name
4-Methylpyridazine, 97%
Brand Name
J&K
Product Number
580354
CAS
1120-88-3
Molecular Formula
C5H6N2
Molecular Weight
94.11
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
136882
IUPAC Name
4-methylpyridazine
InChI Key
AIKUBOPKWKZULG-UHFFFAOYSA-N
SMILES
CC1=CN=NC=C1

Properties

Density
1.06
Boiling Point
98-100
Flash Point
106
n20D
1.5170 to 1.5210

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Designed Nanoporous Solids for the Green Production of Vitamins, Fine Chemicals and Renewable Nylons
Publication Name: Topics in Catalysis
Publication Date: 2009-01-07
DOI: 10.1007/s11244-008-9155-3

Oxidation of Methyl Heteroaryls with Molecular Oxygen: A Facile Synthesis of 2-[N-(tert-Butoxycarbonyl)amino]-4-pyridinecarbaldehyde
Publication Name: Synthesis
Publication Date: 2007-08
DOI: 10.1055/s-2007-983817

Synthesis of Substituted Methyl Pyridazine-4-carboxylates via Cycloaddition of Diazomethane to 2,3-Disubstituted 2-Cyclopropenecarboxylic Acids
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2004-07
DOI: 10.1023/b:rujo.0000045198.22692.97

Condensation Reactions
Publication Name: Science of Synthesis
Publication Date: 2004

Introduction of Cyano Groups by the Reissert Reaction
Publication Name: Science of Synthesis
Publication Date: 2004

4-Methylpyridazine, 97%

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