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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-4-carboxylic acid, 3-amino-1-phenyl-, ethyl ester

CCOC(=O)c1cn(nc1N)c1ccccc1 Request for Quotation
Chemical Name: 1H-Pyrazole-4-carboxylic acid, 3-amino-1-phenyl-, ethyl ester
CAS Number: 16078-63-0
Product Number: AG001VCB(AGN-PC-001WRI)
Synonyms:
MDL No:
Molecular Formula: C12H13N3O2
Molecular Weight: 231.2505

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3-amino-1-phenyl-1H-pyrazole-4-carboxylate is a versatile compound commonly used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its ability to participate in a wide range of reactions.In organic synthesis, Ethyl 3-amino-1-phenyl-1H-pyrazole-4-carboxylate can act as a nucleophile in substitution reactions, enabling the introduction of the pyrazole ring system into target molecules. Additionally, its amino and carboxylate functional groups provide routes for further derivatization, allowing for the incorporation of specific functionalities or structural modifications.Furthermore, this compound can serve as a key intermediate in the preparation of biologically active compounds, making it invaluable in medicinal chemistry research. Its structural versatility and reactivity make it a valuable tool for chemists seeking to access complex molecular scaffolds efficiently and selectively.Overall, Ethyl 3-amino-1-phenyl-1H-pyrazole-4-carboxylate plays a crucial role in advancing chemical synthesis by enabling the construction of diverse molecules with tailored properties and functions.