848940-03-4

Basic information

• Product Name: (2S,3R,4S,5S,6R)-2-(4-Allyloxy-phenoxy)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol
• Synonyms: (2S,3R,4S,5S,6R)-2-(4-Allyloxy-phenoxy)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol
• CAS NO: 848940-03-4
• Molecular Weight: 312.32
• Mol File: 848940-03-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,3R,4S,5S,6R)-2-(4-Allyloxy-phenoxy)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4S,5S,6R)-2-(4-Allyloxy-phenoxy)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol(848940-03-4)
• EPA Substance Registry System: (2S,3R,4S,5S,6R)-2-(4-Allyloxy-phenoxy)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol(848940-03-4)

Safety Data

• Hazardous Substances Data: 848940-03-4(Hazardous Substances Data)

Upstream product

• 106-95-6 allyl bromide 
• 497-76-7 arbutin 

Downstream Products

• 848940-04-5 (2S,3R,4S,5R,6R)-2-(4-Allyloxy-phenoxy)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran 
• 848940-06-7 Toluene-4-sulfonic acid 3-[4-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-phenoxy]-propyl ester 
• 848940-07-8 (2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[4-(3-iodo-propoxy)-phenoxy]-tetrahydro-pyran 
• 848940-05-6 3-[4-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-phenoxy]-propan-1-ol 
• 848940-10-3 [4-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-phenoxy]-acetic acid 
• 848940-09-0 [4-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-phenoxy]-acetaldehyde 

Relevant articles and documents

Synthesis of mono-glucose-branched cyclodextrins with a high inclusion ability for doxorubicin and their efficient glycosylation using Mucor hiemalis endo-β-N-acetylglucosaminidase

The mono-glucose-branched cyclodextrins having an appropriate spacer between the β-cyclodextrin and a glucose moiety were synthesized from β-cyclodextrin and arbutin. They had the significantly high association constants for doxorubicin, the anticancer agent, in the range of 10 5-106 M-1, and worked as highly reactive glycosyl acceptors for the transglycosylation reaction by endo-β-N- acetylglucosaminidase of Mucor hiemalis to produce sialo-complex type oligosaccharide-branched cyclodextrins in the high yields of 65-67%.