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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-(6-aminopyridin-2-yl)acetic acid

Nc1cccc(n1)CC(=O)O Request for Quotation
Chemical Name: 2-(6-aminopyridin-2-yl)acetic acid
CAS Number: 339195-51-6
Product Number: AG00CL09(AGN-PC-0749H8)
Synonyms:
MDL No:
Molecular Formula: C7H8N2O2
Molecular Weight: 152.1506

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(6-Aminopyridin-2-yl)acetic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structural properties, $name$ is particularly valued for its ability to introduce specific functional groups into organic molecules, thereby enhancing their biological activity or chemical reactivity. In organic synthesis, $name$ can act as a key intermediate during the formation of complex molecules, enabling chemists to streamline the production process and achieve high yields. Additionally, the presence of an amino group in $name$ offers opportunities for selective functionalization, facilitating the design of novel compounds with tailored properties. Overall, the strategic incorporation of 2-(6-Aminopyridin-2-yl)acetic acid in chemical reactions demonstrates its significance as a valuable tool for advancing the field of synthetic chemistry.