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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-4-BROMO-6-CHLOROPICOLINIC ACID

Clc1cc(Br)c(c(n1)C(=O)O)N Request for Quotation
Chemical Name: 3-AMINO-4-BROMO-6-CHLOROPICOLINIC ACID
CAS Number: 1073182-90-7
Product Number: AG00HAZ2(AGN-PC-0WAJNP)
Synonyms:
MDL No:
Molecular Formula: C6H4BrClN2O2
Molecular Weight: 251.4652

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-4-bromo-6-chloropicolinic acid, also known as ABCP acid, is a versatile building block commonly utilized in chemical synthesis. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and advanced materials due to its unique structural properties.One key application of 3-Amino-4-bromo-6-chloropicolinic acid is in the synthesis of heterocyclic compounds. By incorporating ABCP acid into reaction pathways, chemists can access a wide range of heterocycles with diverse functionalities and substitution patterns. These heterocyclic structures serve as essential scaffolds in drug discovery and development processes.Furthermore, ABCP acid is frequently employed in the preparation of coordination complexes for catalytic purposes. The presence of both amino and halogen moieties in 3-Amino-4-bromo-6-chloropicolinic acid allows for the formation of stable metal complexes that exhibit unique reactivity profiles. These complexes can catalyze a variety of chemical transformations with high efficiency and selectivity.Additionally, 3-Amino-4-bromo-6-chloropicolinic acid can serve as a key intermediate in the synthesis of functionalized pyridine derivatives. Through strategic derivatization of the amino and halogen functionalities, chemists can access a myriad of structurally diverse pyridine analogs with tailored properties. These modified pyridines find applications in medicinal chemistry, materials science, and organic electronics.In summary, the versatile nature of 3-Amino-4-bromo-6-chloropicolinic acid makes it an indispensable tool in chemical synthesis, enabling the construction of complex molecules with valuable properties and functionalities.