Cas 1356155-30-0,3,4,6-tri-O-acetyl-1,5-anhydro-2-thio-2-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-altritol

1356155-30-0

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Basic information

Product Name: 3,4,6-tri-O-acetyl-1,5-anhydro-2-thio-2-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-altritol
Synonyms: 3,4,6-tri-O-acetyl-1,5-anhydro-2-thio-2-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-altritol
CAS NO:1356155-30-0
Molecular Formula:
Molecular Weight: 636.628
EINECS: N/A
Product Categories: N/A
Mol File: 1356155-30-0.mol
Article Data: 1

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: 3,4,6-tri-O-acetyl-1,5-anhydro-2-thio-2-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-altritol(CAS DataBase Reference)
NIST Chemistry Reference: 3,4,6-tri-O-acetyl-1,5-anhydro-2-thio-2-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-altritol(1356155-30-0)
EPA Substance Registry System: 3,4,6-tri-O-acetyl-1,5-anhydro-2-thio-2-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-altritol(1356155-30-0)

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: 1356155-30-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1356155-30-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,1,5 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1356155-30:
(9*1)+(8*3)+(7*5)+(6*6)+(5*1)+(4*5)+(3*5)+(2*3)+(1*0)=150
150 % 10 = 0
So 1356155-30-0 is a valid CAS Registry Number.

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1356155-30-0Relevant articles and documents

Free-radical hydrothiolation of glycals: A thiol-ene-based synthesis of S-disaccharides

Staderini, Samuele,Chambery, Angela,Marra, Alberto,Dondoni, Alessandro

, p. 702 - 704 (2012)

A method for the synthesis of a new family of 1-deoxy S-disaccharides has been established via free-radical hydrothiolation of glycals by sugar thiols (thiol-ene coupling). The photoinduced coupling between four tri-O-acetyl-d-glycals and three different sugar thiols reveals that the reaction efficiency and stereoselectivity are highly dependent on the stereochemistry of the OAc groups at C3 and C4 of the glycal.

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