Cas 729596-95-6,phenyl 2,3-di-O-benzyl-4,6-di-O-methylsulfonyl-1-thio-β-D-galactopyranoside

729596-95-6

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Basic information

Product Name: phenyl 2,3-di-O-benzyl-4,6-di-O-methylsulfonyl-1-thio-β-D-galactopyranoside
Synonyms: phenyl 2,3-di-O-benzyl-4,6-di-O-methylsulfonyl-1-thio-β-D-galactopyranoside
CAS NO:729596-95-6
Molecular Formula:
Molecular Weight: 608.755
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: phenyl 2,3-di-O-benzyl-4,6-di-O-methylsulfonyl-1-thio-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 2,3-di-O-benzyl-4,6-di-O-methylsulfonyl-1-thio-β-D-galactopyranoside(729596-95-6)
EPA Substance Registry System: phenyl 2,3-di-O-benzyl-4,6-di-O-methylsulfonyl-1-thio-β-D-galactopyranoside(729596-95-6)

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: 729596-95-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 729596-95-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,9,5,9 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 729596-95:
(8*7)+(7*2)+(6*9)+(5*5)+(4*9)+(3*6)+(2*9)+(1*5)=226
226 % 10 = 6
So 729596-95-6 is a valid CAS Registry Number.

729596-95-6Upstream product

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729596-95-6Relevant academic research and scientific papers

Glycosylation of cyclitols: Synthesis of neamine-type aminoglycosides

Verhelst, Steven H. L.,Magnee, Lisette,Wennekes, Tom,Wiedenhof, Wouter,Van Der Marel, Gijsbert A.,Overkleeft, Herman S.,Van Boeckel, Constant A. A.,Van Boom, Jacques H.

, p. 2404 - 2410 (2004)

In this paper, a glycosylation-based approach towards novel aminoglycoside analogues is presented. Three different cyclitol building blocks were condensed with different thioglycosides to give, after removal of the protective groups, several neamine-type

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