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Usage

Uses

Used in Organic Synthesis:
Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside is used as a building block in organic synthesis for constructing more complex molecules. Its unique structure and functional groups make it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside is used as a precursor for the development of new drugs. Its potential applications include the synthesis of pharmaceutical compounds with novel therapeutic properties and improved pharmacological profiles.
Used in Agrochemical Industry:
Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside is also utilized in the agrochemical industry as a precursor for the development of new crop protection agents. Its unique structure and functional groups can be employed to create agrochemicals with enhanced efficacy and selectivity.
Used in Carbohydrate Chemistry:
In the field of carbohydrate chemistry, Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside is used for the study and manipulation of carbohydrate structures and functions. Its unique structure allows researchers to explore the properties and interactions of carbohydrates in various biological systems.
Used in Glycobiology:
Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside has potential utility in glycobiology, where it can be employed to investigate the role of carbohydrates in biological processes and their interactions with other biomolecules. This knowledge can contribute to the development of new therapeutic strategies and diagnostic tools based on carbohydrate biology.

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 
• 114284-06-9 allyl 4-O-benzoyl-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 
• 311779-16-5 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-2,3-di-O-benzoyl-α-L-rhamnopyranose 
• 311779-15-4 allyl (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3-di-O-benzoyl-α-L-rhamnopyranoside 
• 311779-08-5 methyl (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->4)-α-L-rhamnopyranosyl-(1->3)-2-acetamido-2-deoxy-β-D-glucopyranoside 
• 311779-07-4 methyl (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->4)-α-L-rhamnopyranosyl-(1->3)-2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 311779-18-7 (2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 311779-05-2 methyl (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->4)-(2,3-di-O-benzoyl-α-L-rhamnopyranosyl)-(1->3)-2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 89821-78-3 allyl 4-O-benzyl-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 

Relevant academic research and scientific papers

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).

The Allyl Group for Protection in Carbohydrate Chemistry. Part 19. The Coupling of Allyl 2,3-Di-O-methyl-4-O-(3,6-di-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside to Bovine Serum Albumin. Preparation of a Diagnostic Reagent for Antibodies to the Major Glycolipid of Mycobacterium...

Epoxidation of allyl 4-O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-L-rhamnopyranoside and subsequent alkaline hydrolysis of the epoxide and hydrogenolysis of the benzyl groups gave 2',3'-dihydroxypropyl 2,3-di-O-methyl-4-O-(3,6-di-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside which was cleaved with sodium metaperiodate to give the corresponding formylmethyl glycoside.Two other routes to the latter compound, via allyl 2,3-di-O-methyl-4-O-(3,6-di-O-methyl-β-D-glucopyranosyl)-α-L-rhamnopyranoside, were also developed.The formylmethyl glycoside was coupled to bovine serum albumin using 'reductive amination' in the presence of sodium cyanoborohydride to give a glycoconjugate useful for the serodiagnosis of antibodies to the major glycolipid of Mycobacterium leprae in the sera of leprosy patients. 5',6'-Dihydroxyhexyl and 10',11'-dihydroxyundecyl 3,6-di-O-methyl-β-D-glucopyranosides were also prepared as intermediates for the synthesis of the 4-formylbutyl and 9-formylnonyl glucosides respectively which are also suitable for coupling to bovine serum albumin by the 'reductive amination' technique.