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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)-

Propanoic acid, 2,3-dihydroxy-2-methyl-, methyl ester, (2S)-

C[C@@](C(=O)OC)(CO)O Request for Quotation
Chemical Name: Propanoic acid, 2,3-dihydroxy-2-methyl-, methyl ester, (2S)-
CAS Number: 147501-85-7
Product Number: AG001EXP(AGN-PC-0O3J8K)
Synonyms:
MDL No:
Molecular Formula: C5H10O4
Molecular Weight: 134.1305

Identification/Properties

Computed Properties
Molecular Weight:
134.131g/mol
XLogP3:
-1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
134.058g/mol
Monoisotopic Mass:
134.058g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
112
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (2S)-2,3-Dihydroxy-2-methyl-propanoic acid methyl ester, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structural properties make it a valuable intermediate in the creation of various organic compounds. By serving as a chiral precursor, $name$ enables the synthesis of complex molecules with high stereochemical purity. In addition, its hydroxyl groups and methyl functionality make it a key component in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Furthermore, the ester group in $name$ provides diverse reactivity, allowing for the efficient formation of bonds and the modification of functional groups in target molecules. Ultimately, the application of (2S)-2,3-Dihydroxy-2-methyl-propanoic acid methyl ester in chemical synthesis underscores its importance in the development of innovative and structurally diverse compounds.