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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)-

MethylmalonicAcid-d3

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Chemical Name: MethylmalonicAcid-d3
CAS Number: 42522-59-8
Product Number: AG00C5JI(AGN-PC-0WAG1L)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
121.106g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
121.045g/mol
Monoisotopic Mass:
121.045g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
103
Isotope Atom Count:
3
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methylmalonic Acid-d3 is a stable, deuterium-labeled form of Methylmalonic Acid, a key compound in the biosynthesis of succinyl-CoA. Its unique isotopic composition makes it a valuable tool in chemical synthesis, particularly in the study of metabolic pathways and enzyme kinetics. By incorporating Methylmalonic Acid-d3 into synthetic processes, researchers can track the movements of methyl groups within molecules, aiding in the identification of reaction mechanisms and the elucidation of complex biochemical pathways. This isotopically labeled compound offers a precise method for investigating carbon transformations, making it indispensable in the field of organic chemistry and biochemistry.