Cas 913619-28-0,1,3:4,6-di-O-benzylidene-2,5-dideoxy-1,5-[[(2R,3R)-2,4-O-benyzlidene-2,4-dihydroxy-3-(sulfooxy)butyl]sulfoniumylidene]-L-iditol inner salt

913619-28-0

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Basic information

Product Name: 1,3:4,6-di-O-benzylidene-2,5-dideoxy-1,5-[[(2R,3R)-2,4-O-benyzlidene-2,4-dihydroxy-3-(sulfooxy)butyl]sulfoniumylidene]-L-iditol inner salt
Synonyms: 1,3:4,6-di-O-benzylidene-2,5-dideoxy-1,5-[[(2R,3R)-2,4-O-benyzlidene-2,4-dihydroxy-3-(sulfooxy)butyl]sulfoniumylidene]-L-iditol inner salt
CAS NO:913619-28-0
Molecular Formula:
Molecular Weight: 628.721
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: 1,3:4,6-di-O-benzylidene-2,5-dideoxy-1,5-[[(2R,3R)-2,4-O-benyzlidene-2,4-dihydroxy-3-(sulfooxy)butyl]sulfoniumylidene]-L-iditol inner salt(CAS DataBase Reference)
NIST Chemistry Reference: 1,3:4,6-di-O-benzylidene-2,5-dideoxy-1,5-[[(2R,3R)-2,4-O-benyzlidene-2,4-dihydroxy-3-(sulfooxy)butyl]sulfoniumylidene]-L-iditol inner salt(913619-28-0)
EPA Substance Registry System: 1,3:4,6-di-O-benzylidene-2,5-dideoxy-1,5-[[(2R,3R)-2,4-O-benyzlidene-2,4-dihydroxy-3-(sulfooxy)butyl]sulfoniumylidene]-L-iditol inner salt(913619-28-0)

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: 913619-28-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 913619-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,6,1 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 913619-28:
(8*9)+(7*1)+(6*3)+(5*6)+(4*1)+(3*9)+(2*2)+(1*8)=170
170 % 10 = 0
So 913619-28-0 is a valid CAS Registry Number.

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913619-28-0Relevant academic research and scientific papers

Synthesis of new analogues of salacinol containing a pendant hydroxymethyl group as potential glycosidase inhibitors

Nasi, Ravindranath,Pinto, B. Mario

, p. 2305 - 2311 (2007/10/03)

The synthesis of new analogues of the naturally occurring glycosidase inhibitor, salacinol, and its ammonium analogue, ghavamiol is described. These analogues contain an additional hydroxymethyl group at C-1, which was intended to form additional polar co

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