905278-03-7

Basic information

• Product Name: 2-O-benzoyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate
• Synonyms: 2-O-benzoyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate
• CAS NO: 905278-03-7
• Molecular Weight: 592.903
• Mol File: 905278-03-7.mol

Chemical Properties

• CAS DataBase Reference: 2-O-benzoyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-benzoyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate(905278-03-7)
• EPA Substance Registry System: 2-O-benzoyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate(905278-03-7)

Safety Data

• Hazardous Substances Data: 905278-03-7(Hazardous Substances Data)

Upstream product

• 172296-66-1 Phenyl 3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 98-88-4 benzoyl chloride 
• 545-06-2 trichloroacetonitrile 

Downstream Products

• 1025071-01-5 C₄₈H₅₂O₁₀ 
• 1025071-02-6 C₄₃H₄₈O₁₁ 
• 905278-05-9 ethyl (2-O-benzoyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-benzoyl-4-O-benzyl-1-thio-α-L-rhamnopyranoside 

Relevant articles and documents

Synthetic Routes toward Acidic Pentasaccharide Related to the O-Antigen of E. coli 120 Using One-Pot Sequential Glycosylation Reactions

Concise syntheses of the acidic pentasaccharide, related to the O-antigenic polysaccharide of Escherichia coli 120, as its p-methoxyphenyl glycoside, have been achieved using a one-pot sequential glycosylation technique. The glycosylations have been accom

Synthesis of pentasaccharide fragments related to the O-specific polysaccharide of Shigella flexneri serotype 1a

The synthesis of the pentasaccharide 5-aminopentyl glycosides α-L-Rhap-(1→3)-[α-D-Glcp-(1→4)]-β-D-GlcpNAc- (1→2)-α-L-Rhap-(1→2)-α-L-Rhap-1-O-(CH2) 5NH2 (29) and α-L-Rhap-(1→3)-α-L-Rhap- (1→3)-[α-D-Glcp-(1→4)]-β-D-GlcpNAc-(1→2) -α-L-Rhap-1-O-(CH2)5NH2 (28), related to the O-specific polysaccharide of Shigella ilexneri serotype 1a by coupling of the suitably protected trisaccharides α-D-Glcp-(1→4)-β-D- Glcp(1→2)-α-L-Rhap-1-O-(CH2)5NH2 (23) and α-L-Rhap-(1→3)-[α-D-Glcp-(1→4)]-β-D-Glcp-1- SPh (26) with the corresponding rhamnosyl glycosides α-L-Rhap-(1→3)- α-L-Rhap-1-SEt (17) and α-L-Rhap-(1→3)-α-L-Rhap-1-O- (CH2)5NH2 (13), is described. Building blocks 23 and 26 were prepared by intramolecular glycosylation of an unsymmetrically tethered cellobiosamine derivative. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.