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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, 5-amino-1-(phenylmethyl)-, ethyl ester

CCOC(=O)c1cnn(c1N)Cc1ccccc1 Request for Quotation
Chemical Name: 1H-Pyrazole-4-carboxylic acid, 5-amino-1-(phenylmethyl)-, ethyl ester
CAS Number: 19867-62-0
Product Number: AG002BOM(AGN-PC-0O6UEJ)
Synonyms:
MDL No:
Molecular Formula: C13H15N3O2
Molecular Weight: 245.2771

Identification/Properties

Properties
BP:
424.943°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
245.282g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
245.116g/mol
Monoisotopic Mass:
245.116g/mol
Topological Polar Surface Area:
70.1A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
279
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 5-amino-1-benzyl-1H-pyrazole-4-carboxylate is a versatile compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows it to participate in a variety of reactions, leading to the synthesis of complex molecules with diverse functionalities.In organic synthesis, Ethyl 5-amino-1-benzyl-1H-pyrazole-4-carboxylate can be utilized in the formation of heterocyclic compounds through cyclization reactions. It can also serve as a key intermediate in the preparation of substituted pyrazoles, which are important structural motifs found in numerous biologically active compounds. Additionally, this compound may be employed in the synthesis of peptides and amino acid derivatives, contributing to the development of novel drug candidates.Furthermore, Ethyl 5-amino-1-benzyl-1H-pyrazole-4-carboxylate can be functionalized to introduce various functional groups, enabling chemists to tailor its properties for specific applications. Its compatibility with a wide range of reaction conditions makes it a valuable tool for designing and constructing complex molecular frameworks in organic synthesis.