93714-02-4

Basic information

• Product Name: 2-Propenoic acid, 3-(2,2-dimethyl-1,3-dioxolan-4-yl)-2-methyl-, ethyl ester, (Z)-
• CAS NO: 93714-02-4
• Molecular Formula: C11H18O4
• Molecular Weight: 214.262
• Mol File: 93714-02-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-(2,2-dimethyl-1,3-dioxolan-4-yl)-2-methyl-, ethyl ester, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-(2,2-dimethyl-1,3-dioxolan-4-yl)-2-methyl-, ethyl ester, (Z)-(93714-02-4)
• EPA Substance Registry System: 2-Propenoic acid, 3-(2,2-dimethyl-1,3-dioxolan-4-yl)-2-methyl-, ethyl ester, (Z)-(93714-02-4)

Safety Data

• Hazardous Substances Data: 93714-02-4(Hazardous Substances Data)

Upstream product

• 3699-66-9 ethyl 2-diethoxyphosphorylpropionate 
• 5736-03-8 (d,l) isopropylidene glyceraldehyde 
• 535-11-5 Ethyl 2-bromopropionate 
• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 21382-82-1 (carbethoxyethylidene)triphenylphosphorane 
• 22323-80-4 (4S)-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 1707-77-3 1,2:5,6-di-O-isopropylidene-D-mannitol 

Downstream Products

• 93635-76-8 (2S,3R)-3-[(4R)-2,2-dimethyl-[1,3]dioxolane-4-yl]-2,3-dihydroxy-2-methylpropionic acid ethyl ester 
• 93635-77-9 C₂₇H₂₂O₈ 
• 7392-74-7 C₂₇H₂₂O₈ 
• 7392-74-7 C₂₇H₂₂O₈ 
• 23709-41-3 2,3-O-isopropylidene-2-C-methyl-DL-ribono-1,4-lactone 
• 23709-41-3 2,3-O-isopropylidene-2-C-methyl-DL-lyxono-1,4-lactone 
• 492-30-8 2-C-methyl-DL-ribono-1,4-lactone 
• 492-30-8 2-C-methyl-DL-lyxono-1,4-lactone 
• 93636-26-1 ethyl 4,5-O-isopropylidene-2-C-methyl-D-xylonate 
• 93635-76-8 ethyl 4,5-O-isopropylidene-2-C-methyl-DL-lyxonate 
• 93635-76-8 ethyl 4,5-O-isopropylidene-2-C-methyl-DL-ribonate 

Relevant articles and documents

Preparation method of 2-C-methyl-4, 5-O-(1-methylvinyl)-D-arabitic acid ethyl ester

The invention discloses a preparation method of 2-C-methyl-4, 5-O-(1-methylvinyl)-D-arabitic acid ethyl ester (formula I). Compared with the prior art, the preparation method has short reaction steps,reduces the use of organic solvents and generation of solid waste. At the same time, the used reagents are all conventional reagents, the method has the characteristics of simple operation, mild reaction conditions and environmental friendliness, and can achieve industrial preparation of 2-C-methyl-4, 5-O-(1-methylvinyl)-D-arabitic acid ethyl ester.

Synthesis of 5-Hydroxymethyl-3-methylfuran-2(5H)-one

5-hydroxymethyl-3-methylfuran-2(5H)-one,the intermediate in the synthesis of lepiochlorin, was prepared by hydrolysis of ethyl (Z)-3-(2,2-dimethyl-1,3-dioxane-4-yl)-2-propenoate resulting from condensation of 2,3-O-isopropylideneglyceraldehyde with ethyl 2-diethoxyphosphinoylpropionate.