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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)-

2-Methoxypropionic acid

CC(C(=O)O)OC Request for Quotation
Chemical Name: 2-Methoxypropionic acid
CAS Number: 4324-37-2
Product Number: AG003793(AGN-PC-0WA6WJ)
Synonyms:
MDL No:
Molecular Formula: C4H8O3
Molecular Weight: 104.1045

Identification/Properties

Properties
BP:
199.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
104.105g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
104.047g/mol
Monoisotopic Mass:
104.047g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
69.3
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H312-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methoxypropanoic acid, also known as methyl lactate, is a versatile chemical compound widely used in chemical synthesis processes. One of its key applications is as a solvent in various reactions due to its high solvency power and low toxicity. Additionally, 2-Methoxypropanoic acid is utilized as a reagent in esterification reactions to form esters, a common process in organic chemistry. Its ability to act as a carboxylic acid derivative makes it a valuable intermediate in the synthesis of pharmaceuticals, fragrances, and other complex organic compounds. Furthermore, 2-Methoxypropanoic acid can also serve as a building block in the production of polymers and resins, adding to its importance in industrial applications.