Cas 528861-64-5,1-{methyl (4S,5R)-2,3,6-tri-O-benzyl-4-deoxy-α-L-threo-hexopyranosid[4,5-b]-2-methyl-1,4-oxathiin-3-yl}ethanone

528861-64-5

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Basic information

Product Name: 1-{methyl (4S,5R)-2,3,6-tri-O-benzyl-4-deoxy-α-L-threo-hexopyranosid[4,5-b]-2-methyl-1,4-oxathiin-3-yl}ethanone
Synonyms: 1-{methyl (4S,5R)-2,3,6-tri-O-benzyl-4-deoxy-α-L-threo-hexopyranosid[4,5-b]-2-methyl-1,4-oxathiin-3-yl}ethanone
CAS NO:528861-64-5
Molecular Formula:
Molecular Weight: 576.711
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-{methyl (4S,5R)-2,3,6-tri-O-benzyl-4-deoxy-α-L-threo-hexopyranosid[4,5-b]-2-methyl-1,4-oxathiin-3-yl}ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-{methyl (4S,5R)-2,3,6-tri-O-benzyl-4-deoxy-α-L-threo-hexopyranosid[4,5-b]-2-methyl-1,4-oxathiin-3-yl}ethanone(528861-64-5)
EPA Substance Registry System: 1-{methyl (4S,5R)-2,3,6-tri-O-benzyl-4-deoxy-α-L-threo-hexopyranosid[4,5-b]-2-methyl-1,4-oxathiin-3-yl}ethanone(528861-64-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 528861-64-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 528861-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,8,8,6 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 528861-64:
(8*5)+(7*2)+(6*8)+(5*8)+(4*6)+(3*1)+(2*6)+(1*4)=185
185 % 10 = 5
So 528861-64-5 is a valid CAS Registry Number.

528861-64-5Upstream product

528861-64-5Downstream Products

161016-86-0 methyl 2,3,6-tri-O-benzyl-4-deoxy-α-L-threo-hex-4-enopyranoside

528861-64-5Relevant academic research and scientific papers

Conformational evaluation of some 4-deoxyhex-4-enopyranose derivatives and their use in the preparation of a previously undescribed class of 3-thio-L-sorbopyranosides and their 6-C-methoxy analogues

Capozzi, Giuseppe,Catelani, Giorgio,D'Andrea, Felicia,Menichetti, Stefano,Nativi, Cristina

, p. 123 - 132 (2003)

A new series of thio-substituted sugars were synthesised relying on the totally regio- and stereoselective cycloaddition of 4-deoxyhex-4-enopyranose derivatives to 'in situ' generated oxothiones. Conformational studies of the above unsaturated sugars showed a marked prevalence of the all-axial conformer.

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