CAS 72657-23-9
:(R)-(-)-methyl B-hydroxyisobutyrate
Description:
(R)-(-)-Methyl β-hydroxyisobutyrate, with the CAS number 72657-23-9, is an organic compound characterized by its chiral structure, which includes a hydroxyl group and a methyl ester functional group. This compound is a derivative of isobutyric acid and is known for its role in various biochemical processes, particularly in the context of metabolic pathways. It is typically a colorless to pale yellow liquid with a pleasant odor, and it is soluble in water and organic solvents. The presence of the hydroxyl group contributes to its reactivity, allowing it to participate in various chemical reactions, including esterification and oxidation. As a chiral molecule, it exists in two enantiomeric forms, with the (R)-(-) configuration being of particular interest in pharmaceutical applications due to its potential biological activity. This compound is often used in research and development, particularly in the synthesis of other chiral compounds and in studies related to metabolic regulation and energy production.
Formula:C5H10O3
InChI:InChI=1/C5H10O3/c1-4(3-6)5(7)8-2/h4,6H,3H2,1-2H3/t4-/m0/s1
SMILES:C[C@@H](CO)C(=O)OC
Synonyms:- ()-Methyl D-beta-hydroxyisobutyrate
- Methyl (R)-()-3-hydroxy-2-methylpropionate
- (R)-(-)-3-hydroxy-2-methylpropionic*acid methyl E
- (R)-(-)-3-Hydroxyisobutyric acid methyl ester
- methyl (2R)-3-hydroxy-2-methyl-propanoate
- methyl (2S)-3-hydroxy-2-methylpropanoate
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Found 6 products.
Methyl (R)-(-)-3-Hydroxyisobutyrate
CAS:Formula:C5H10O3Purity:>99.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:118.13Methyl (R)-(-)-3-hydroxy-2-methylpropionate
CAS:Formula:C5H10O3Purity:96%Color and Shape:LiquidMolecular weight:118.1311(R)-(-)-3-Hydroxy-2-methylpropionic acid methyl ester
CAS:<p>(R)-(-)-3-Hydroxy-2-methylpropionic acid methyl ester</p>Formula:C5H10O3Purity:96%Color and Shape: clear. colourless liquidMolecular weight:118.13g/mol(R)-3-Hydroxyisobutyric Acid Methyl Ester
CAS:Controlled Product<p>Applications Chiral derivative of 3-Hydroxyisobutyrate.<br>References Waldmann, H., et al.: Bioorg. Med. Chem., 2, 477 (1994), Vonstein, V., et al.: J. Bacteriol., 177, 4540 (1995),<br></p>Formula:C5H10O3Color and Shape:NeatMolecular weight:118.13(R)-Methyl 3-hydroxy-2-methylpropanoate
CAS:Formula:C5H10O3Purity:96%Color and Shape:Liquid, ClearMolecular weight:118.132(R)-3-Hydroxyisobutyric acid methyl ester
CAS:<p>(R)-3-Hydroxyisobutyric acid methyl ester is a retronecine analogue that can be synthesized by hydrozirconation of an (R)-3-hydroxyisobutyryl chloride. The synthesis starts with the stereoselective formation of an acid lactone from a chiral intramolecular Diels-Alder reaction between a cyclic enol ether and a butenolide. This lactone is then converted to the desired product by lactonization followed by anion formation and mismatch elimination. The final step involves alkylation of the olefin with methyllithium, followed by acid hydrolysis to give the desired product.</p>Formula:C5H10O3Purity:Min. 95%Molecular weight:118.13 g/mol





