Cas 728899-98-7,(1R,4S,5R,6S)-4,5-dibenzyloxy-1-benzyloxymethyl-6-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyloxy)cyclohex-2-en-1-ol

728899-98-7

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Basic information

Product Name: (1R,4S,5R,6S)-4,5-dibenzyloxy-1-benzyloxymethyl-6-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyloxy)cyclohex-2-en-1-ol
Synonyms: (1R,4S,5R,6S)-4,5-dibenzyloxy-1-benzyloxymethyl-6-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyloxy)cyclohex-2-en-1-ol
CAS NO:728899-98-7
Molecular Formula:
Molecular Weight: 877.044
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: (1R,4S,5R,6S)-4,5-dibenzyloxy-1-benzyloxymethyl-6-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyloxy)cyclohex-2-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,4S,5R,6S)-4,5-dibenzyloxy-1-benzyloxymethyl-6-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyloxy)cyclohex-2-en-1-ol(728899-98-7)
EPA Substance Registry System: (1R,4S,5R,6S)-4,5-dibenzyloxy-1-benzyloxymethyl-6-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyloxy)cyclohex-2-en-1-ol(728899-98-7)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 728899-98-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 728899-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,8,8,9 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 728899-98:
(8*7)+(7*2)+(6*8)+(5*8)+(4*9)+(3*9)+(2*9)+(1*8)=247
247 % 10 = 7
So 728899-98-7 is a valid CAS Registry Number.

728899-98-7Upstream product

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728899-98-7Relevant academic research and scientific papers

Some approaches to glycosylated versions of methyl β-acarviosin

Fairweather, Jon K.,McDonough, Matthew J.,Stick, Robert V.,Tilbrook, D. Matthew G.

, p. 197 - 205 (2007/10/03)

In a first approach to a glycosylated version of 'methyl β-acarviosin', a putative inhibitor of cellulases, cellobiose was converted into a carbocyclic enone that could not be transformed into the required amine for a subsequent alkylation. Alternatively,

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