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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)-

Propanedioic acid, amino-

NC(C(=O)O)C(=O)O Request for Quotation
Chemical Name: Propanedioic acid, amino-
CAS Number: 1068-84-4
Product Number: AG0082UZ(AGN-PC-0JLCCZ)
Synonyms:
MDL No:
Molecular Formula: C3H5NO4
Molecular Weight: 119.0761

Identification/Properties

Computed Properties
Molecular Weight:
119.076g/mol
XLogP3:
-3.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
119.022g/mol
Monoisotopic Mass:
119.022g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
107
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Aminomalonic acid is a versatile compound that finds extensive applications in chemical synthesis due to its unique structural properties and reactivity. With a primary amine group and two carboxylic acid groups, Aminomalonic acid serves as a valuable building block for the synthesis of various complex molecules and materials. In organic chemistry, Aminomalonic acid is commonly employed as a precursor for the preparation of amino acids, peptides, and polyamides through condensation reactions. Furthermore, its ability to participate in multicomponent reactions allows for the efficient synthesis of diverse heterocyclic compounds and drug candidates. The resulting products exhibit enhanced biological activities and structural diversity, making Aminomalonic acid an essential reagent in pharmaceutical research and drug discovery. In material science, Aminomalonic acid derivatives are utilized for the fabrication of functional polymers, coatings, and biomaterials with tailored properties such as biocompatibility, adhesion, and thermal stability. Overall, the strategic incorporation of Aminomalonic acid in chemical synthesis enables the rapid and efficient assembly of molecular architectures with high precision and control, advancing the frontiers of synthetic organic chemistry and materials science.