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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)-

3-Pyridinecarboxylic acid, 6-chloro-2-cyclopropyl-

OC(=O)c1ccc(nc1C1CC1)Cl Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-chloro-2-cyclopropyl-
CAS Number: 862695-75-8
Product Number: AG00IDZK(AGN-PC-0D5BK4)
Synonyms:
MDL No:
Molecular Formula: C9H8ClNO2
Molecular Weight: 197.6183

Identification/Properties

Computed Properties
Molecular Weight:
197.618g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
197.024g/mol
Monoisotopic Mass:
197.024g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
218
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-2-cyclopropylnicotinic acid is a valuable intermediate in chemical synthesis due to its unique structural properties and versatile reactivity. Primarily utilized in pharmaceutical and agrochemical industries, this compound serves as a key building block in the synthesis of various biologically active molecules.One of the significant applications of 6-Chloro-2-cyclopropylnicotinic acid is in the development of novel pharmaceutical agents. Its cyclopropyl moiety imparts distinctive steric and electronic characteristics that can enhance the biological activity and metabolic stability of drug candidates. By incorporating this acid into the molecular structure of potential medicines, chemists can modulate the pharmacokinetic properties and optimize the therapeutic efficacy of the final products.Furthermore, this compound plays a crucial role in the synthesis of pesticides and herbicides. The chloro substituent on the pyridine ring can act as a directing group in various chemical transformations, facilitating the introduction of additional functional groups at specific positions. By manipulating the reactivity of 6-Chloro-2-cyclopropylnicotinic acid through selective reactions, chemists can access a diverse array of pesticide molecules with tailored properties for pest control and agricultural applications.