111219-29-5

Basic information

• Product Name: Benzeneacetic acid, (2,2-dimethyl-1,3-dioxolan-4-yl)methyl ester
• CAS NO: 111219-29-5
• Molecular Formula: C14H18O4
• Molecular Weight: 250.295
• Mol File: 111219-29-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, (2,2-dimethyl-1,3-dioxolan-4-yl)methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, (2,2-dimethyl-1,3-dioxolan-4-yl)methyl ester(111219-29-5)
• EPA Substance Registry System: Benzeneacetic acid, (2,2-dimethyl-1,3-dioxolan-4-yl)methyl ester(111219-29-5)

Safety Data

• Hazardous Substances Data: 111219-29-5(Hazardous Substances Data)

Upstream product

• 100-79-8 (R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol 
• 1555-80-2 phenylacetic anhydride 
• 103-80-0 phenylacetyl chloride 

Downstream Products

• 22323-82-6 (S)-(+)-(2,2-dimethyl-[1,3]dioxolan-4-yl)methanol 
• 14347-78-5 1,2-O-isopropylidene-D-glycerol 

Relevant articles and documents

Synthesis of glycerolipids containing simple linear acyl chains or aromatic rings and evaluation of their Mincle signaling activity

Mincle, expressed in activated phagocytes, recognizes the lipid ligand to activate the innate immune system. We have synthesized glycerol derivatives possessing simple alkyl chains or aromatic rings and elucidated their structure-activity relationships us

Lipase-mediated desymmetrization of glycerol with aromatic and aliphatic anhydrides

Chirazyme L-2 (Candida antarctica) catalyzed esterification of glycerol with aromatic and aliphatic anhydrides in 1,4-dioxane is described. All the aromatic monoacylglycerols (MAGs) were produced as (R)-enantiomers, while aliphatic MAGs were obtained either as racemic mixtures or the (S)-enantiomers. The influence of substituted aromatic rings, chain length, and presence of a conjugated double bond in the acyl donor moiety on the enantiotopic selectivity as well as the efficiency of the enzyme was studied.