62999-50-2

Basic information

• Product Name: 1,3-Dioxolane, 4-ethenyl-2-phenyl-
• CAS NO: 62999-50-2
• Molecular Formula: C11H12O2
• Molecular Weight: 176.215
• Mol File: 62999-50-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxolane, 4-ethenyl-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolane, 4-ethenyl-2-phenyl-(62999-50-2)
• EPA Substance Registry System: 1,3-Dioxolane, 4-ethenyl-2-phenyl-(62999-50-2)

Safety Data

• Hazardous Substances Data: 62999-50-2(Hazardous Substances Data)

Usage

Chemical structure

A six-membered carbon ring with two oxygen atoms at opposite positions, a vinyl group, and a phenyl group.

Functional groups

1,3-Dioxolane ring, vinyl group, phenyl group

Physical state

Liquid at room temperature

Solvent properties

High solvency power

Industrial applications

Used in various industrial and research applications

Health hazards

Potential health hazards, should be handled with care

Flammability

Flammable

Reactivity

Low reactivity

Toxicity

Low toxicity

Safety measures

Proper handling and storage required to minimize health and safety risks

Synthesis

Used in chemical synthesis processes

Extraction

Utilized in extraction processes

Upstream product

• 497-06-3 3,4-butenediol 
• 100-52-7 benzaldehyde 
• 930-22-3 epoxybutene 

Downstream Products

• 103160-49-2 1,2-O,O'-bisdecanoyl-3-O-benzyl-rac-glycerol 
• 13071-59-5 3-benzyloxypropan-1,2-diol 
• 1708-39-0 1,2-benzylideneglycerol 
• 108826-60-4 2-Phenyl-[1,3]dioxolane-4-carbaldehyde 

Relevant articles and documents

Fragrance and/or flavoring compositions containing dioxolanes

The present invention primarily relates to the use of dioxolanes of the following Formula (I) as fragrance and/or flavoring substances, certain perfume and/or flavoring compositions comprising these dioxolanes and corresponding perfumed and/or flavored items. The present invention also relates to a method for producing the dioxolanes of Formula (I) and certain new dioxolanes according to Formula (I).

New synthesis of sn-1,2- and sn-2,3-O-diacylglycerols application to the synthesis of enantiopure phosphonates analogous to triglycerides: A new class of inhibitors of lipases

Phosphonate compounds mimic the first transition state occurring during enzymatic carboxyester hydrolysis of natural substrates by forming a covalent bond with the catalytic serine. However, until now the organophosphorus compounds used in the inhibition studies more or less resembled a natural triglyceride substrate. In order to elucidate the interfacial activation and the mechanism of action of lipases, specific inhibitors need to be prepared. To achieve this goal, enantiomerically pure sn-1,2- and sn-2,3O- didecanoylglycerol compounds were prepared - starting from a C-4 chiral synthon, 3-buten-1,2-diol - and treated with n-pentylphosphonic dichloride and p-nitrophenol to afford the corresponding diastereomeric phosphonates, which were acylglycerol analogs. Subsequent separation of each of the phosphonate diastereomers A/B or ent-A/ent-B, performed by HPLC, led to four enantiopure stereoisomers that will be investigated as inhibitors of Human Pancreatic Lipase (HPL) and Human Gastric Lipase (HGL) using the monomolecular film technique.