Cas 215653-60-4,methyl 4,6-O-benzylidene-2-S-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-thio-α-D-mannopyranoside

215653-60-4

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Basic information

Product Name: methyl 4,6-O-benzylidene-2-S-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-thio-α-D-mannopyranoside
Synonyms:
CAS NO:215653-60-4
Molecular Formula:
Molecular Weight: 628.651
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: methyl 4,6-O-benzylidene-2-S-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-thio-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4,6-O-benzylidene-2-S-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-thio-α-D-mannopyranoside(215653-60-4)
EPA Substance Registry System: methyl 4,6-O-benzylidene-2-S-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-thio-α-D-mannopyranoside(215653-60-4)

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: 215653-60-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 215653-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,6,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 215653-60:
(8*2)+(7*1)+(6*5)+(5*6)+(4*5)+(3*3)+(2*6)+(1*0)=124
124 % 10 = 4
So 215653-60-4 is a valid CAS Registry Number.

215653-60-4Upstream product

19879-84-6 2,3,4,6-tetra-O-acetyl-1-thio-α-D-mannopyranoside

215653-60-4Downstream Products

215653-60-4Relevant academic research and scientific papers

Synthesis of heteroanalogues of disaccharides as potential inhibitors of the processing mannosidase Class I enzymes

Johnston, Blair D.,Pinto, B. Mario

, p. 17 - 25 (2007/10/03)

Three disaccharide analogues of α-D-Man-(1→2)-α-D-Man-OMe in which the ring and/or glycosidic oxygen atoms have been replaced by sulfur have been synthesized as potential inhibitors of Class I mannosidase enzymes. Glycosylation of appropriately protected

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