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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)-

Benzoic acid, 4-(1H-pyrazol-1-yl)-, ethyl ester

CCOC(=O)c1ccc(cc1)n1cccn1 Request for Quotation
Chemical Name: Benzoic acid, 4-(1H-pyrazol-1-yl)-, ethyl ester
CAS Number: 143426-47-5
Product Number: AG003Q8Q(AGN-PC-0JYS9V)
Synonyms:
MDL No: MFCD05994003
Molecular Formula: C12H12N2O2
Molecular Weight: 216.2359

Identification/Properties

Properties
BP:
333.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
216.24g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
216.09g/mol
Monoisotopic Mass:
216.09g/mol
Topological Polar Surface Area:
44.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
237
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


Ethyl 4-(1-Pyrazolyl)benzoate is a versatile compound widely used in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials.The presence of the pyrazole ring in Ethyl 4-(1-Pyrazolyl)benzoate imparts unique chemical reactivity, making it an important intermediate in the production of heterocyclic compounds. The pyrazole moiety allows for diverse functionalization and modification, enabling the creation of complex molecules with specific properties.In organic synthesis, Ethyl 4-(1-Pyrazolyl)benzoate can be utilized in the construction of biologically active compounds, such as antiviral agents, anti-inflammatory drugs, and enzyme inhibitors. Its structural features make it a valuable substrate for the development of novel chemical entities with potential pharmaceutical applications.Furthermore, the versatile nature of Ethyl 4-(1-Pyrazolyl)benzoate facilitates its use in the synthesis of chiral compounds and asymmetric catalysis. Its compatibility with various reaction conditions and functional groups makes it a valuable tool for chemists striving to access diverse molecular architectures.Overall, Ethyl 4-(1-Pyrazolyl)benzoate plays a crucial role in modern synthetic chemistry, enabling the efficient and strategic construction of complex molecules with diverse applications in medicinal chemistry, material science, and chemical biology.