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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)-

3-methoxyoxolane-3-carboxylic acid

COC1(COCC1)C(=O)O Request for Quotation
Chemical Name: 3-methoxyoxolane-3-carboxylic acid
CAS Number: 1204831-21-9
Product Number: AG01BCXF(AGN-PC-0WOT6P)
Synonyms:
MDL No:
Molecular Formula: C6H10O4
Molecular Weight: 146.1412

Identification/Properties

Computed Properties
Molecular Weight:
146.142g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
146.058g/mol
Monoisotopic Mass:
146.058g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
145
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


3-Methoxyoxolane-3-carboxylic acid is a versatile compound commonly used in chemical synthesis for its unique properties and applications. This organic acid plays a crucial role in various chemical reactions, particularly in the pharmaceutical and agricultural industries.1. Synthesis of Pharmaceutical Intermediates:
3-Methoxyoxolane-3-carboxylic acid is frequently employed as a precursor in the synthesis of pharmaceutical intermediates. Its functional groups and structural characteristics make it suitable for the creation of complex molecules used in drug development. By reacting with other reagents and compounds, this acid enables the production of key pharmaceutical building blocks with specific biological activities.2. Asymmetric Synthesis:
The chiral nature of 3-Methoxyoxolane-3-carboxylic acid makes it a valuable reagent in asymmetric synthesis. Its three-dimensional arrangement of atoms allows for the creation of enantiomerically pure compounds, crucial in the pharmaceutical industry to ensure the desired biological activity and minimize potential side effects. Chemists utilize this acid to generate stereochemically complex molecules with high selectivity.3. Agrochemical Development:
In the field of agrochemicals, 3-Methoxyoxolane-3-carboxylic acid finds application in the synthesis of active ingredients for pesticides, herbicides, and fungicides. The acid's chemical structure can be modified to introduce specific functional groups that enhance the efficacy and selectivity of agricultural chemicals. By incorporating this compound into the synthesis of agrochemical products, researchers can tailor the properties of these compounds to maximize their agricultural benefits.Overall, 3-Methoxyoxolane-3-carboxylic acid serves as a valuable reagent in chemical synthesis, particularly in pharmaceutical and agrochemical applications. Its versatility, chiral nature, and functional groups make it an essential building block for the creation of diverse compounds with targeted properties and activities.