71695-57-3

Basic information

• Product Name: Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside
• Synonyms: Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside;Allyl 2,3-O-isopropylidene-alpha-L-rhamnopyranoside
• CAS NO: 71695-57-3
• Molecular Formula: C₁₂H₂₀O₅
• Molecular Weight: 244.2842
• Mol File: 71695-57-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside(71695-57-3)
• EPA Substance Registry System: Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside(71695-57-3)

Safety Data

• Hazardous Substances Data: 71695-57-3(Hazardous Substances Data)

Usage

General Description

Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside is a chemical compound that belongs to the family of rhamnopyranosides. It is a derivative of a-L-rhamnose, a type of sugar, and contains an allyl group and an isopropylidene protecting group. Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside is commonly used in organic synthesis and chemical research as a building block for the synthesis of more complex molecules. It has potential applications in the pharmaceutical and agrochemical industries as a precursor for the development of new drugs and crop protection agents. Additionally, it may also have potential utility in the field of carbohydrate chemistry and glycobiology for the study and manipulation of carbohydrate structures and functions.

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 
• 112254-88-3 allyl 2,3-O-isopropylidene-4-O-(4-methoxybenzyl)-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 
• 1133712-73-8 allyl 2,3-O-isopropylidene-4-O-(p-methoxybenzoyl)-α-L-rhamnopyranoside 
• 384371-55-5 2^D,3^D,5^D-Tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranosyl 2,2,2-trichloroacetimidate 
• 384371-53-3 Allyl 2^D,3^D,5^D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranoside 
• 516516-81-7 C₅₃H₅₄O₂₂ 
• 384371-52-2 Allyl 2',3',5'-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-2-O-benzoyl-α-L-rhamnopyranoside 
• 384371-51-1 C₃₅H₃₆O₁₂ 
• 526209-01-8 allyl 2,3,4-tri-O-benzoyl-β-L-xylopyranosyl-(1-> 4)-α-L-rhamnopyranoside 
• 541503-05-3 allyl 3-O-acetyl-2,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 541503-07-5 allyl 2,4-di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranosyl-(1->2)-3-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside 
• 541503-06-4 allyl 2,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzoyl-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).