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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)-

Butanoic acid, 4-[(5-bromo-2-pyridinyl)amino]-4-oxo-

O=C(Nc1ccc(cn1)Br)CCC(=O)O Request for Quotation
Chemical Name: Butanoic acid, 4-[(5-bromo-2-pyridinyl)amino]-4-oxo-
CAS Number: 188011-69-0
Product Number: AG00ABN5(AGN-PC-0JUB5I)
Synonyms:
MDL No:
Molecular Formula: C9H9BrN2O3
Molecular Weight: 273.0834

Identification/Properties

Computed Properties
Molecular Weight:
273.086g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
271.98g/mol
Monoisotopic Mass:
271.98g/mol
Topological Polar Surface Area:
79.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
248
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-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-[(5-Bromo-2-pyridinyl)amino]-4-oxobutanoic acid is a versatile compound used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various organic molecules due to its functional groups and reactivity. In particular, the 4-[(5-Bromo-2-pyridinyl)amino]-4-oxobutanoic acid is often employed in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its ability to undergo selective chemical reactions makes it a crucial intermediate in the production of complex organic compounds with specific biological or industrial activities. Scientists and researchers rely on the 4-[(5-Bromo-2-pyridinyl)amino]-4-oxobutanoic acid to facilitate the synthesis of target molecules efficiently and effectively, highlighting its significance in advancing modern chemistry and drug discovery efforts.