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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, 3,4-diamino-4-oxo-, (3R)-

OC(=O)C[C@H](C(=O)N)N Request for Quotation
Chemical Name: Butanoic acid, 3,4-diamino-4-oxo-, (3R)-
CAS Number: 200260-37-3
Product Number: AG002CMB(AGN-PC-0O6ZOW)
Synonyms:
MDL No:
Molecular Formula: C4H8N2O3
Molecular Weight: 132.1179

Identification/Properties

Computed Properties
Molecular Weight:
132.119g/mol
XLogP3:
-4.5
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
132.053g/mol
Monoisotopic Mass:
132.053g/mol
Topological Polar Surface Area:
106A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
134
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-3,4-Diamino-4-oxobutanoic acid is a versatile compound widely utilized in chemical synthesis for its distinctive properties and reactivity. As a key intermediate in organic chemistry, this compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a valuable building block for the synthesis of peptidomimetics, amino acids, and heterocyclic compounds, offering a wide range of applications in drug discovery and development. Additionally, (R)-3,4-Diamino-4-oxobutanoic acid is commonly employed as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiopure compounds with high stereoselectivity. Its significance in chemical synthesis lies in its ability to facilitate the construction of complex molecular structures with enhanced efficiency and precision.