50721-02-3

Basic information

• Product Name: (1R,3S,4R,5S,8S)-4,8-bis(benzyloxy)-3-methoxy-2,6-dioxabicyclo[3.2.1]octane
• Synonyms: (1R,3S,4R,5S,8S)-4,8-bis(benzyloxy)-3-methoxy-2,6-dioxabicyclo[3.2.1]octane
• CAS NO: 50721-02-3
• Molecular Weight: 356.419
• Mol File: 50721-02-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (1R,3S,4R,5S,8S)-4,8-bis(benzyloxy)-3-methoxy-2,6-dioxabicyclo[3.2.1]octane(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,3S,4R,5S,8S)-4,8-bis(benzyloxy)-3-methoxy-2,6-dioxabicyclo[3.2.1]octane(50721-02-3)
• EPA Substance Registry System: (1R,3S,4R,5S,8S)-4,8-bis(benzyloxy)-3-methoxy-2,6-dioxabicyclo[3.2.1]octane(50721-02-3)

Safety Data

• Hazardous Substances Data: 50721-02-3(Hazardous Substances Data)

Upstream product

• 4356-80-3 methyl 2,3,4-tri-O-benzyl-α-D-galactopyranoside 
• 167013-68-5 methyl 2,3,4-tri-O-benzyl-6-O-(p-toluenesulfonyl)-α-D-galactopyranoside 
• 88713-83-1 methyl 2,3,4-tri-O-benzyl-6-O-(methylsulfonyl)-α-D-galactopyranoside 
• 5540-31-8 methyl 3,6-anhydro-α-D-galactopyranoside 
• 100-39-0 benzyl bromide 

Relevant articles and documents

RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo

We synthesized ten new analogs of 6′-modified KRN7000 (A): RCAI-58, 61, 64, 83, 85-87, 113, 119, and 125. They could be synthesized by α-selective galactosylation of ceramide 9 with the 6-modified d-galactopyranosyl fluorides (8a-8f) or l-arabinopyranosyl

The first synthesis of secondary sugar sulfonic acids by nucleophilic displacement reactions

The 4-deoxy-4-C-sulfonic acid and 6-deoxy-6-C-sulfonic acid derivatives of methyl α-D-gluco- and α-D-galactopyranosides were prepared by triflate-mediated nucleophilic displacement reactions, either with NaHSO 3 or with AcSK. The triflate ester

Synthesis and conformational studies of carrabiose and its 4'-sulphate and 2,4'-disulphate

Methyl α-carrabioside (13), and its 4'-sulphate (19) and 2,4'-disulphate (20) have been synthesized via glycosylation of methyl 3,6-anhydro-2-O-benzyl-α-D-galactopyranoside with 2,3,6-tri-O-acetyl-4-O-benzyl-β-D-galactopyranosyl bromide and subsequent par