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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)-

4-Chloro-2-methylnicotinic acid

OC(=O)c1c(Cl)ccnc1C Request for Quotation
Chemical Name: 4-Chloro-2-methylnicotinic acid
CAS Number: 914219-06-0
Product Number: AG006B19(AGN-PC-0WAG6L)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO2
Molecular Weight: 171.5810

Identification/Properties

Computed Properties
Molecular Weight:
171.58g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
171.009g/mol
Monoisotopic Mass:
171.009g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
163
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-2-methylnicotinic acid is a versatile compound that finds wide application in chemical synthesis processes. Its unique structure and properties make it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. When 4-Chloro-2-methylnicotinic acid is used in chemical syntheses, it serves as a key intermediate in the production of numerous important organic compounds.One prominent application of 4-Chloro-2-methylnicotinic acid is in the synthesis of heterocyclic compounds. These compounds play a crucial role in drug discovery and development, as they often exhibit diverse biological activities. By incorporating 4-Chloro-2-methylnicotinic acid into the chemical synthesis of heterocycles, researchers can access a wide range of novel molecules with potential pharmacological properties.Additionally, 4-Chloro-2-methylnicotinic acid can be employed in the preparation of functionalized organic molecules through various synthetic routes. Its presence in the synthesis pathway can enable the introduction of specific functional groups or structural motifs, thereby influencing the properties of the final compound. This flexibility makes 4-Chloro-2-methylnicotinic acid a valuable tool for chemists seeking to tailor the characteristics of their target molecules.Overall, the use of 4-Chloro-2-methylnicotinic acid in chemical synthesis offers a strategic approach to accessing structurally diverse compounds with potential applications in various industries. Its role as a versatile intermediate highlights its importance in the development of new materials and bioactive molecules.