100639-25-6

Basic information

• Product Name: allyl 2,3-O-isopropylidene-α-D-rhamnopyranoside
• CAS NO: 100639-25-6
• Molecular Weight: 244.288
• Mol File: 100639-25-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: allyl 2,3-O-isopropylidene-α-D-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 2,3-O-isopropylidene-α-D-rhamnopyranoside(100639-25-6)
• EPA Substance Registry System: allyl 2,3-O-isopropylidene-α-D-rhamnopyranoside(100639-25-6)

Safety Data

• Hazardous Substances Data: 100639-25-6(Hazardous Substances Data)

Upstream product

• 112254-88-3 allyl 2,3-O-isopropylidene-4-O-(4-methoxybenzyl)-α-L-rhamnopyranoside 

Downstream Products

• 89821-77-2 Allyl 4-O-benzyl-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 384371-50-0 Allyl 2',3',5'-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 236731-57-0 allyl (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 155165-96-1 Allyl 4-O-acetyl-3-O-(4-methoxybenzyl)-α-L-rhamnopyranoside 
• 155165-97-2 Allyl 4-O-acetyl-2-O-benzoyl-3-O-(4-methoxybenzyl)-α-L-rhamnopyranoside 
• 1392506-96-5 [2,3,4-tri-O-benzyl-β-D-xylopyranosyl-(1->4)]-2,3-di-O-isopropylidene-L-rhamnopyranose 
• 1392506-97-6 [2,3,4-tri-O-benzyl-β-D-xylopyranosyl-(1->4)]-2,3-di-O-isopropylidene-L-rhamnopyranose 
• 1072450-37-3 trichloroacetimidoyl 2,3,4-tri-O-benzyl-β-D-xylopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-xylopyranosyl-(1->4)-2,3-di-O-isopropylidene-α-L-rhamnopyranoside 
• 1072450-36-2 triisopropylsilyl 2,3,4-tri-O-benzyl-β-D-xylopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-xylopyranosyl-(1->4)-2,3-di-O-isopropylidene-α-L-rhamnopyranoside 
• 1026022-17-2 O-triisopropylsilyl {[5-O-benzyl-2,3-di-O-benzylidene-β-D-apiofuranosyl-(1->3)]-2,4-di-O-benzyl-β-D-xylopyranosyl-(1->4)}-2,3-di-O-isopropylidene-α-L-rhamnopyranoside 

Relevant articles and documents

Structurally Simple Benzyl-Type Photolabile Protecting Groups for Direct Release of Alcohols and Carboxylic Acids

Structurally simple benzyl-type photolabile protecting groups (PPGs) have been developed to release alcohols and carboxylic acids. Release of two substrates from one PPG chromophore has also been accomplished. (Chemical Equation Presented).