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1,3-Dimethyl-1H-pyrazole-5-amine, 97%|100155|3524-32-1

1,3-Dimethyl-1H-pyrazole-5-amine, 97%

Cat. No JKH09028_5_G
J&K Chemical

Product Information

Product Name
1,3-Dimethyl-1H-pyrazole-5-amine, 97%
Brand Name
J&K
Product Number
100155
CAS
3524-32-1
Molecular Formula
C5H9N3
Molecular Weight
111.15
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
520721
IUPAC Name
2,5-dimethylpyrazol-3-amine
InChI Key
ZFDGMMZLXSFNFU-UHFFFAOYSA-N
SMILES
CC1=NN(C(=C1)N)C

Properties

Melting Point
65-69
Flash Point
88

Safety Information

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

Iodine-Promoted Oxidative Carbonylation
Publication Name: Science of Synthesis
Publication Date: 2024

Dehydrative Coupling of Indole-Activated Alcohols and Amines
Publication Name: Science of Synthesis
Publication Date: 2024

5(4)-Aminopyrazoles as effective reagents in the synthesis of pyrazolo-annulated pyridines
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2022-05-31
DOI: 10.1007/s10593-022-03069-8

Palladium-catalyzed amino group arylation of 1,3-disubstituted 1H-pyrazol-5-amine based on Buchwald–Hartwig reaction
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2021-06-26
DOI: 10.1007/s10593-021-02961-z

Efficient Route for the Synthesis of Diverse Heteroannelated 5-Cyanopyridines
Publication Name: Synthesis
Publication Date: 2021-02-08
DOI: 10.1055/a-1360-9852

1,3-Dimethyl-1H-pyrazole-5-amine, 97%

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