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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Pyrazole-3-carboxylic acid, 4-amino-5-methyl-

OC(=O)c1[nH]nc(c1N)C Request for Quotation
Chemical Name: 1H-Pyrazole-3-carboxylic acid, 4-amino-5-methyl-
CAS Number: 94993-81-4
Product Number: AG005TL6(AGN-PC-0JQ9G6)
Synonyms:
MDL No:
Molecular Formula: C5H7N3O2
Molecular Weight: 141.1280

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
141.13g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
141.054g/mol
Monoisotopic Mass:
141.054g/mol
Topological Polar Surface Area:
92A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
150
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-Amino-3-methyl-1H-pyrazole-5-carboxylic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique properties. In organic chemistry, this compound serves as a crucial building block for the construction of various heterocyclic compounds, pharmaceuticals, and agrochemicals. Its reactive amino and carboxylic acid groups enable it to participate in a range of synthetic reactions, including amide formation, condensation reactions, and cyclization processes. Additionally, the presence of the methyl group provides additional flexibility in molecular design, making it a valuable tool for fine-tuning the properties of synthesized compounds in drug discovery and material science applications.