107914-61-4

Basic information

• Product Name: 2,3-Dihydro-3-oxo-2,5-diphenyl-4-(3,4,5-tri-O-acetyl-2,6-anhydro-L-galactonoyloxy)thiophen-1,1-dioxid
• CAS NO: 107914-61-4
• Molecular Weight: 586.573
• Mol File: 107914-61-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,3-Dihydro-3-oxo-2,5-diphenyl-4-(3,4,5-tri-O-acetyl-2,6-anhydro-L-galactonoyloxy)thiophen-1,1-dioxid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Dihydro-3-oxo-2,5-diphenyl-4-(3,4,5-tri-O-acetyl-2,6-anhydro-L-galactonoyloxy)thiophen-1,1-dioxid(107914-61-4)
• EPA Substance Registry System: 2,3-Dihydro-3-oxo-2,5-diphenyl-4-(3,4,5-tri-O-acetyl-2,6-anhydro-L-galactonoyloxy)thiophen-1,1-dioxid(107914-61-4)

Safety Data

• Hazardous Substances Data: 107914-61-4(Hazardous Substances Data)

Upstream product

• 103730-04-7 Brom-2,3,4-tri-O-acetyl-α-D-galactopyranosiduronsaeure 
• 54714-11-3 4,6-diphenylthieno-[3,4-d]-1,3-dioxol-2-one-5,5-dioxide 
• 107914-60-3 3,4,5-Tri-O-acetyl-2,6-anhydro-L-galactonsaeure 

Downstream Products

• 107914-65-8 N-(3,4,5-Tri-O-acetyl-2,6-anhydro-L-galactonoyl)-DL-2-phenylglycin-(3-methyl-2-butenyl)ester 
• 118437-23-3 (E)-N-(3,4,5-Tri-O-acetyl-2,6-anhydro-L-galactonoyl)-DL-2-phenylglycin-cinnamylester 
• 118437-22-2 (E)-N-(3,4,5-Tri-O-acetyl-2,6-anhydro-L-galactonoyl)-DL-2-phenylglycin-(2-methylcinnamylester) 
• 107914-70-5 2-(3-Methyl-2-butenyl)-4-phenyl-2-(2,3,4-tri-O-acetyl-β-L-lyxopyranosyl)-5(2H)-oxazolon 
• 107914-75-0 2-(2-Oxoethyl)-4-phenyl-2-(2,3,4-tri-O-acetyl-β-L-lyxopyranosyl)-5(2H)-oxazolon 
• 118437-25-5 (E)-2-Cinnamyl-4-phenyl-2-(2,3,4-tri-O-acetyl-β-L-lyxopyranosyl)-5(2H)-oxazolon 
• 118437-28-8 <(E)-Cinnamyl><2,3,4-tri-O-acetyl-β-L-lyxopyranosyl>keton 

Relevant articles and documents

Chain Elongation of Carbohydrates: Synthesis of Pyrazoles from Optically Active Carboxylic Acids

By chain elongation via the C-phenylglycine method optically active carboxylic acids may be converted into 3-substituted pyrazoles in few steps with good chemical yields.Starting with peracetylated glyconic acids this technique permits an easy access to u