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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-methoxy-, ethyl ester

CCOC(=O)C(OC)C Request for Quotation
Chemical Name: Propanoic acid, 2-methoxy-, ethyl ester
CAS Number: 4324-39-4
Product Number: AG00DFI3(AGN-PC-0JQDF0)
Synonyms:
MDL No:
Molecular Formula: C6H12O3
Molecular Weight: 132.15768

Identification/Properties

Computed Properties
Molecular Weight:
132.159g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
132.079g/mol
Monoisotopic Mass:
132.079g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
90.3
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


Ethyl 2-methoxypropanoate, also known as ethyl methylglycolate, serves as a versatile building block in the realm of chemical synthesis. This compound is commonly utilized as a reagent in organic reactions, particularly in the formation of diverse esters and carboxylic acid derivatives. Due to its unique chemical structure, ethyl 2-methoxypropanoate enables the introduction of methoxy and ethoxy functional groups into various organic molecules, making it a valuable tool in the synthesis of pharmaceuticals, fragrances, and other fine chemicals. Its compatibility with a wide range of solvents and reaction conditions further enhances its utility in the laboratory, facilitating the efficient creation of novel compounds with tailored properties.