2-(1-ETHYL-1H-PYRAZOL-3-YL)ACETIC ACID|1172566-04-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

2-(1-ETHYL-1H-PYRAZOL-3-YL)ACETIC ACID

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Chemical Name:	2-(1-ETHYL-1H-PYRAZOL-3-YL)ACETIC ACID
CAS Number:	1172566-04-9
Product Number:	AG00HDWD(AGN-PC-0WAJZR)
Synonyms:
MDL No:
Molecular Formula:	C7H10N2O2
Molecular Weight:	154.1665

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Chemical Structure

The 2-(1-ethyl-1H-pyrazol-3-yl)acetic acid is an essential reagent in chemical synthesis, particularly in the field of organic chemistry. It serves as a versatile building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. This compound is commonly employed as a precursor in the synthesis of bioactive molecules due to its unique structural properties. With its functional groups and reactivity, this compound facilitates the formation of complex molecular structures through various organic reactions such as esterification, amidation, and condensation reactions. Its use in chemical synthesis enables the creation of new compounds with diverse applications in medicinal chemistry, materials science, and other related fields.