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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)-

5-ethyl-1H-pyrazole-4-carboxylic acid

CCc1n[nH]cc1C(=O)O Request for Quotation
Chemical Name: 5-ethyl-1H-pyrazole-4-carboxylic acid
CAS Number: 1007541-72-1
Product Number: AG0002TM(AGN-PC-03X8TV)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O2
Molecular Weight: 140.1399

Identification/Properties

Computed Properties
Molecular Weight:
140.142g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
140.059g/mol
Monoisotopic Mass:
140.059g/mol
Topological Polar Surface Area:
66A^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

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


5-Ethyl-1H-pyrazole-4-carboxylic acid is a versatile compound widely utilized in chemical synthesis due to its unique structure and reactivity. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. With its carboxylic acid functionality, 5-Ethyl-1H-pyrazole-4-carboxylic acid can participate in a range of important synthetic reactions such as amidation, esterification, and coupling reactions. Additionally, its pyrazole ring offers opportunities for further functionalization through substitution or modifications, allowing for the creation of novel molecules with tailored properties. In the field of medicinal chemistry, 5-Ethyl-1H-pyrazole-4-carboxylic acid can be used as a key intermediate in the synthesis of bioactive compounds, demonstrating its significance in drug discovery and development.