133337-03-8

Basic information

• Product Name: (4S,5S)-4-Benzyl-5-but-3-enyl-2,2-dimethyl-[1,3]dioxolane
• CAS NO: 133337-03-8
• Molecular Weight: 246.349
• Mol File: 133337-03-8.mol

Chemical Properties

• CAS DataBase Reference: (4S,5S)-4-Benzyl-5-but-3-enyl-2,2-dimethyl-[1,3]dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-4-Benzyl-5-but-3-enyl-2,2-dimethyl-[1,3]dioxolane(133337-03-8)
• EPA Substance Registry System: (4S,5S)-4-Benzyl-5-but-3-enyl-2,2-dimethyl-[1,3]dioxolane(133337-03-8)

Safety Data

• Hazardous Substances Data: 133337-03-8(Hazardous Substances Data)

Upstream product

• 133337-02-7 ((4S,5S)-5-But-3-enyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol 
• 133337-02-7 (2R,3R)-2,3-isopropylidendioxy-6-hepten-1-ol 
• 70831-49-1 (4S,5S)-4-hydroxymethyl-2,2-dimethyl-5-tosyloxymethyl-1,3-dioxolane 
• 23402-69-9 lithium diphenylcuprate 
• 128162-83-4 Toluene-4-sulfonic acid (4S,5S)-2,2-dimethyl-5-trifluoromethanesulfonyloxymethyl-[1,3]dioxolan-4-ylmethyl ester 
• 1730-25-2 allylmagnesium bromide 
• 73711-65-6 (4R,5R)-<5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolane-4-yl>methyl p-toluenesulfonate 

Downstream Products

• 145761-24-6 (5S,1'S)-5-(1'-methanesulfonyloxy-2'-phenylethyl)dihydrofuran-2(3H)-one 
• 133337-04-9 Acetic acid (R)-1-((S)-5-oxo-tetrahydro-furan-2-yl)-2-phenyl-ethyl ester 
• 125225-52-7 (5S,1'S)-5-(1'-hydroxy-2'-phenylethyl)dihydrofuran-2(3H)-one 
• 125225-51-6 (5S,1'R)-5-(1'-hydroxy-2'-phenylethyl)dihydrofuran-2(3H)-one 
• 140844-93-5 3-((4S,5S)-5-Benzyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-propionaldehyde 
• 145761-24-6 Methanesulfonic acid (R)-1-((R)-5-oxo-tetrahydro-furan-2-yl)-2-phenyl-ethyl ester 
• 151692-01-2 3-((4R,5R)-5-Benzyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-propionic acid 
• 133337-04-9 Acetic acid (S)-1-((R)-5-oxo-tetrahydro-furan-2-yl)-2-phenyl-ethyl ester 
• 125225-53-8 (R)-5-((S)-1-Hydroxy-2-phenyl-ethyl)-dihydro-furan-2-one 
• 125225-54-9 (4R,5R)-5-hydroxy-6-phenyl-4-hexanolide 
• 140844-93-5 3-((4R,5R)-5-Benzyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-propionaldehyde 

Relevant articles and documents

Synthesis of Lateral Root-Inducing Compounds Using an Efficient Coupling Reaction of Chiral Triflates

Lateral root-inducing compounds, isolated from the bacterium Erwinia quercina, have been synthesized by using a coupling reaction of chiral triflates derived from L- or D-tartrates and their biological activities examined.