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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-hydroxy-3-methoxy-, methyl ester

COCC(C(=O)OC)O Request for Quotation
Chemical Name: Propanoic acid, 2-hydroxy-3-methoxy-, methyl ester
CAS Number: 54927-70-7
Product Number: AG01AD0C(AGN-PC-043LTZ)
Synonyms:
MDL No:
Molecular Formula: C5H10O4
Molecular Weight: 134.1305

Identification/Properties

Computed Properties
Molecular Weight:
134.131g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
134.058g/mol
Monoisotopic Mass:
134.058g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
91
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


Methyl 2-hydroxy-3-methoxypropanoate, also known as methyl glycolate, serves as a valuable building block in chemical synthesis. This compound is commonly utilized in the production of pharmaceuticals, agrochemicals, flavors, and fragrances. Its unique chemical structure makes it a versatile intermediate in organic reactions, allowing for the formation of a variety of complex molecules.In chemical synthesis, methyl 2-hydroxy-3-methoxypropanoate can participate in esterification, acylation, and condensation reactions to construct more intricate organic compounds. Its hydroxyl and ester groups provide sites for further functionalization, enabling the introduction of various functional groups to tailor the properties of the final product. Additionally, the presence of the methoxy group offers opportunities for selective transformations, enhancing the specificity of the synthetic route.Overall, methyl 2-hydroxy-3-methoxypropanoate plays a crucial role in the synthesis of diverse chemical compounds due to its reactivity, compatibility with different functional groups, and ability to undergo various chemical transformations.