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Ethyl 3-amino-4-pyrazolecarboxylate, 99%|167515|6994-25-8

Ethyl 3-amino-4-pyrazolecarboxylate, 99%

Cat. No JK167515_5_G
J&K Chemical

Product Information

Product Name
Ethyl 3-amino-4-pyrazolecarboxylate, 99%
Brand Name
J&K
Product Number
167515
CAS
6994-25-8
Molecular Formula
C6H9N3O2
Molecular Weight
155.15
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
3-Amino-4-carboethoxy-1H-pyrazole
PubChem CID
81472
IUPAC Name
ethyl 5-amino-1H-pyrazole-4-carboxylate
InChI Key
YPXGHKWOJXQLQU-UHFFFAOYSA-N
SMILES
CCOC(=O)C1=C(NN=C1)N

Properties

Melting Point
105-107

Safety Information

Signal Word
Warning
Hazard Statement
H317
H410
Precautionary Statement
P261
P272
P280
P321
P501
P273
P391
P302+P352
P333+P317
P362+P364

References Data Source From Pubchem

Photocatalytic Fluoroalkylation of Derivatives of 3-Aminopyrazole
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2025-06
DOI: 10.1134/s1070428025602262

Repotrectinib
Publication Name: Pharmaceutical Substances
Publication Date: 2025

A synthesis of novel 5-methylsulfanylazolo[1,5-a]pyrimidin-7(4H)-ones and investigation of their chemical and cytotoxic properties
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2024-02
DOI: 10.1007/s10593-024-03293-4

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells
Publication Name: Biochemical and Biophysical Research Communications
Publication Date: 2023-10-30
DOI: 10.1016/j.bbrc.2023.08.050

Diversity-oriented synthesis of 1H-1,2,3-triazole tethered pyrazolo[5,1-b]quinazoline hybrids as antimicrobial agents
Publication Name: Molecular Diversity
Publication Date: 2023-09-11
DOI: 10.1007/s11030-023-10721-8

Ethyl 3-amino-4-pyrazolecarboxylate, 99%

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