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1,3,5-Trimethyl-1H-pyrazole-4-carboxaldehyde, 97%|904145|2644-93-1

1,3,5-Trimethyl-1H-pyrazole-4-carboxaldehyde, 97%

Cat. No JK904145_250_MG
J&K Chemical

Product Information

Product Name
1,3,5-Trimethyl-1H-pyrazole-4-carboxaldehyde, 97%
Brand Name
J&K
Product Number
904145
CAS
2644-93-1
Molecular Formula
C7H10N2O
Molecular Weight
138.17
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
736515
IUPAC Name
1,3,5-trimethylpyrazole-4-carbaldehyde
InChI Key
HMTUBXVXHHITGO-UHFFFAOYSA-N
SMILES
CC1=C(C(=NN1C)C)C=O

Properties

Melting Point
80-83
Boiling Point
132

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

On-DNA Cyclization To Give Benzimidazoles
Publication Name: Science of Synthesis
Publication Date: 2024

Quantum-chemical study of mechanisms of reaction between 1,3,5-trimethyl-1H-pyrazole-4-carbaldehyde with 2-mercaptoethanol
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2013-02
DOI: 10.1134/s1070428013020164

Condensation of Arylaldehydes with α-Azido-Esters
Publication Name: Science of Synthesis
Publication Date: 2007

Vilsmeier-Haak formylation of 3,5-dimethylpyrazoles
Publication Name: Russian Journal of General Chemistry
Publication Date: 2006-11
DOI: 10.1134/s1070363206110260

Electrosynthesis of 1,3,5-Trimethylpyrazole-4-Carboxylic Acid through Oxidation of 1,3,5-Trimethyl-4-Formylpyrazoles on a Nickel Anode in Aqueous Alkaline Medium
Publication Name: Russian Journal of Electrochemistry
Publication Date: 2005-10
DOI: 10.1007/s11175-005-0194-9

1,3,5-Trimethyl-1H-pyrazole-4-carboxaldehyde, 97%

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