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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)-

B007158, 2-(4-Methylpyrazol-1-yl)acetic acid

Cc1cn(nc1)CC(=O)O Request for Quotation
Chemical Name: B007158, 2-(4-Methylpyrazol-1-yl)acetic acid
CAS Number: 956364-44-6
Product Number: AG00IJ9X(AGN-PC-0WALXU)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O2
Molecular Weight: 140.1399

Identification/Properties

Computed Properties
Molecular Weight:
140.142g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
140.059g/mol
Monoisotopic Mass:
140.059g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
138
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Methyl-1H-pyrazol-1-yl)acetic acid, also known as $name$, is a valuable compound in chemical synthesis. This versatile molecule acts as a key building block in organic chemistry, particularly in the formation of heterocyclic structures. In chemical synthesis, $name$ is commonly utilized as a starting material for the creation of novel pharmaceuticals, agrochemicals, and materials. Its unique structure containing a pyrazole ring allows for the synthesis of diverse compounds with desired properties. One of the primary applications of 2-(4-Methyl-1H-pyrazol-1-yl)acetic acid is in the preparation of bioactive molecules and intermediates. By functionalizing the pyrazole moiety, chemists can introduce specific functional groups to tailor the properties of the final compound. This enables the customization of molecules for a variety of applications, such as drug discovery and materials science. Moreover, the presence of the acetic acid group in $name$ provides a handle for further derivatization, allowing for the attachment of different substituents to modulate the compound's reactivity and biological activity. Overall, 2-(4-Methyl-1H-pyrazol-1-yl)acetic acid is an essential building block in the toolkit of synthetic chemists for the preparation of diverse and functionalized molecules with applications across various industries.