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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-amino-6-chloro-4-methylpyridine-2-carboxylic acid

Clc1cc(C)c(c(n1)C(=O)O)N Request for Quotation
Chemical Name: 3-amino-6-chloro-4-methylpyridine-2-carboxylic acid
CAS Number: 1073182-76-9
Product Number: AG00HAZ1(AGN-PC-0CVR5Z)
Synonyms:
MDL No:
Molecular Formula: C7H7ClN2O2
Molecular Weight: 186.5957

Identification/Properties

Computed Properties
Molecular Weight:
186.595g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
186.02g/mol
Monoisotopic Mass:
186.02g/mol
Topological Polar Surface Area:
76.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
188
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-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-6-chloro-4-methylpicolinic acid, a versatile compound commonly used in chemical synthesis, is renowned for its significant role in numerous applications across various industries. Due to its unique chemical structure, 3-Amino-6-chloro-4-methylpicolinic acid serves as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and specialty chemicals. Its functional groups make it a valuable building block for creating complex molecules with enhanced properties and functionalities.In pharmaceutical research and development, 3-Amino-6-chloro-4-methylpicolinic acid is utilized to synthesize novel drug candidates, especially those targeting central nervous system disorders and anticancer agents. Its incorporation in the molecular structure of bioactive compounds enhances their biological activity and pharmacokinetic profiles.Furthermore, in the agrochemical industry, this compound plays a crucial role in the production of pesticides, herbicides, and fungicides. By incorporating 3-Amino-6-chloro-4-methylpicolinic acid into the synthesis of these agricultural chemicals, their efficacy and selectivity can be significantly improved, leading to enhanced crop protection and yield.Additionally, the versatility of 3-Amino-6-chloro-4-methylpicolinic acid extends to the realm of specialty chemicals, where it is employed in the development of functional materials, catalysts, and intermediates for various industrial processes. Its reactivity and compatibility with other compounds make it a preferred choice for creating advanced materials with tailored properties and improved performance.In essence, the application of 3-Amino-6-chloro-4-methylpicolinic acid in chemical synthesis encompasses a wide range of industries, contributing to the advancement of pharmaceuticals, agrochemicals, and specialty chemicals through the creation of innovative and high-value products.