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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)-

2-Pyridinecarboxylic acid, 4-ethyl-, hydrochloride

CCc1ccnc(c1)C(=O)O.Cl Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 4-ethyl-, hydrochloride
CAS Number: 79415-18-2
Product Number: AG008M6Q(AGN-PC-00JX30)
Synonyms:
MDL No:
Molecular Formula: C8H10ClNO2
Molecular Weight: 187.6235

Identification/Properties

Computed Properties
Molecular Weight:
187.623g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
187.04g/mol
Monoisotopic Mass:
187.04g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
147
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Ethylpicolinic acid hydrochloride is a versatile compound commonly utilized in chemical synthesis processes. This compound serves as an important building block for the creation of various organic molecules due to its unique structure and reactivity. In organic chemistry, 4-Ethylpicolinic acid hydrochloride is often employed as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It can participate in various reactions, such as nucleophilic substitutions, oxidation reactions, and transition metal catalyzed transformations. The presence of the ethyl group on the picolinic acid scaffold confers specific properties to the compound, making it a valuable intermediate in the preparation of complex organic molecules. Its ability to undergo diverse chemical transformations makes it a valuable tool for synthetic chemists seeking to construct novel compounds for various applications.