Methyl 1-amino-3-methyl-1H-pyrazole-5-carboxylate

Base Information

Chemical Name:Methyl 1-amino-3-methyl-1H-pyrazole-5-carboxylate
CAS No.:150017-57-5
Molecular Formula:C₆H₉N₃O₂
Molecular Weight:155.156
Hs Code.:
DSSTox Substance ID:DTXSID40569166
Wikidata:Q82456256
Mol file:150017-57-5.mol

Synonyms:150017-57-5;Methyl 1-amino-3-methyl-1H-pyrazole-5-carboxylate;METHYL 2-AMINO-5-METHYLPYRAZOLE-3-CARBOXYLATE;1H-Pyrazole-5-carboxylicacid,1-amino-3-methyl-,methylester(9CI);DTXSID40569166

Suppliers and Price of Methyl 1-amino-3-methyl-1H-pyrazole-5-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of Methyl 1-amino-3-methyl-1H-pyrazole-5-carboxylate

Chemical Property:

PSA：70.14000
LogP:0.27310
XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:155.069476538
Heavy Atom Count:11
Complexity:162

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NN(C(=C1)C(=O)OC)N

Technology Process of Methyl 1-amino-3-methyl-1H-pyrazole-5-carboxylate

There total 1 articles about Methyl 1-amino-3-methyl-1H-pyrazole-5-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 25016-17-5
5-methyl-2H-pyrazole-3-carboxylic acid methyl ester

: 1-Amino-5-methylpyrazol-3-carbonsaeure-methylester

: 150017-57-5
1-Amino-3-methylpyrazol-5-carbonsaeure-methylester

Guidance literature:: With diazomethane; sodium hydroxide; hydroxylamine-O-sulfonic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) 1 h, 2.) MeOH, ether;