L-Menthyl 2,2-dihydroxyacetate

CAS : 111969-64-3

Ref. 3D-FM43993

Informations sur le produit

• Nom: L-Menthyl 2,2-dihydroxyacetate
• Synonymes: (1R,2S,5R)-5-Methyl-2-(1-Methylethyl)Cyclohexyl Dihydroxy-Acetate, (1R,2S,5R)-5-Methyl-2-(1-methylethyl)cyclohexyl 2,2-dihydroxyacetate, (1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl dihydroxyacetate, 2,2-Dihydroxyacetic Acid (-)-Menthyl Ester, Acetic acid, 2,2-dihydroxy-, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester, Acetic acid, dihydroxy-, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester, Acetic acid, dihydroxy-, 5-methyl-2-(1-methylethyl)cyclohexyl ester, [1R-(1α,2β,5α)]-, Glyoxylic acid (1S)-menthyl ester hydrate, L-Menthyl glyoxylate hydrate, L-Mgh
• CAS: 111969-64-3

Description

L-Menthyl 2,2-dihydroxyacetate is a synthetic compound that belongs to the group of salicylic acid derivatives. It is an intermediate in the synthesis of other compounds and can be recycled. L-Menthyl 2,2-dihydroxyacetate reacts with primary amines to form iminoacetic esters and glyoxylates by acidic hydrolysis. The reaction time depends on the type of amine and the acidity of the solution. This compound has been used as a reagent to synthesize maleic anhydride from maleic acid. L-Menthyl 2,2-dihydroxyacetate is also used in methodologies for oxidizing aromatic compounds to produce benzoic acids or phenols.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 230.3 g/mol
• Formule: C₁₂H₂₂O₄
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder