124943-18-6

Basic information

• Product Name: allyl 2,4-di-O-benzyl-α-L-rhamnopyranoside
• Synonyms: allyl 2,4-di-O-benzyl-α-L-rhamnopyranoside
• CAS NO: 124943-18-6
• Molecular Weight: 384.472
• Mol File: 124943-18-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: allyl 2,4-di-O-benzyl-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 2,4-di-O-benzyl-α-L-rhamnopyranoside(124943-18-6)
• EPA Substance Registry System: allyl 2,4-di-O-benzyl-α-L-rhamnopyranoside(124943-18-6)

Safety Data

• Hazardous Substances Data: 124943-18-6(Hazardous Substances Data)

Upstream product

• 107-18-6 allyl alcohol 
• 197916-07-7 2-allyloxy-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran 
• 388079-15-0 allyl 3-O-trityl-α-L-rhamnopyranoside 
• 64650-81-3 allyl α-L-rhamnopyranoside 
• 124943-17-5 allyl 2,4-di-O-benzyl-3-O-<<β-(trimethylsilyl)ethoxy>methyl>-α-L-rhamnopyranoside 
• 100-39-0 benzyl bromide 
• 73-34-7 L-rhamnose 

Downstream Products

• 1603826-95-4 allyl (2-O-benzoyl-4-O-benzyl-3-O-para-methoxybenzyl-α-L-rhamnopyranosyl)-(1→2)-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 124943-23-3 allyl 3-O-<3'-O-<<β-(trimethylsilyl)ethoxy>methyl>-4'-O-benzyl-α-L-rhamnopyranosyl>-2,4-di-O-benzyl-α-L-rhamnopyranoside 
• 388079-22-9 allyl O-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)-(1->3)-O-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2,4-di-O-benzyl-α-L-rhamnopyranoside 
• 388079-32-1 allyl O-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)-(1->3)-2,4-di-O-benzyl-α-L-rhamnopyranoside 
• 129926-72-3 allyl 3-O-(2'-O-benzoyl-4'-O-benzyl-3'-O-<2''-deoxy-2''-phthalimido-3'',4'',6''-tris-O-<2-(trimethylsilyl)ethoxymethyl>-β-D-glucopyranosyl>-α-L-rhamnopyranosyl)-2,4-di-O-benzyl-α-L-rhamnopyranoside 
• 124943-20-0 allyl 3-O-<2'-O-benzoyl-3'-O-<<β-(trimethylsilyl)ethoxy>methyl>-4'-O-benzyl-α-L-rhamnopyranosyl>-2,4-di-O-benzyl-α-L-rhamnopyranoside 

Relevant articles and documents

An easy and versatile approach for the regioselective De-O-benzylation of protected sugars based on the I2/Et3SiH combined system

The use of cheap and easy to handle reagents, such as I2 and Et3SiH, at low temperature allows the regioselective removal of benzyl protecting groups from highly O-benzylated carbohydrates. The observed regioselectivity is dependent

Use of the methyl (SEM) Protecting Group in Carbohydrate Chemistry. Fully Functionalized Rhamnose Acceptors and Donors for Use in Oligosaccharide Synthesis

The use of the methyl (SEM) acetal as a protecting group in carbohydrate chemistry is described.The compatibility of this group with a variety of protection/deprotection conditions normally encountered in oligosaccharide synthesi