Cas 487000-70-4,phenyl 2-(N-acetylamino)-3,6-di-O-acetyl-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1-seleno-β-D-glucopyranoside

487000-70-4

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Basic information

Product Name: phenyl 2-(N-acetylamino)-3,6-di-O-acetyl-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1-seleno-β-D-glucopyranoside
Synonyms: phenyl 2-(N-acetylamino)-3,6-di-O-acetyl-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1-seleno-β-D-glucopyranoside
CAS NO:487000-70-4
Molecular Formula:
Molecular Weight: 774.635
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-(N-acetylamino)-3,6-di-O-acetyl-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1-seleno-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 2-(N-acetylamino)-3,6-di-O-acetyl-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1-seleno-β-D-glucopyranoside(487000-70-4)
EPA Substance Registry System: phenyl 2-(N-acetylamino)-3,6-di-O-acetyl-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1-seleno-β-D-glucopyranoside(487000-70-4)

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: 487000-70-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 487000-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,7,0,0 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 487000-70:
(8*4)+(7*8)+(6*7)+(5*0)+(4*0)+(3*0)+(2*7)+(1*0)=144
144 % 10 = 4
So 487000-70-4 is a valid CAS Registry Number.

487000-70-4Upstream product

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487000-70-4Relevant academic research and scientific papers

Galacto, Gluco, Manno, and Disaccharide-Based C-Glycosides of 2-Amino-2-deoxy Sugars

Grant, Laura,Liu, Yan,Walsh, Kenneth E.,Walter, Daryl S.,Gallagher, Timothy

, p. 4623 - 4625 (2007/10/03)

(Matrix Presented) Starting from readily available precursors, selenoglycosides derived from GalNAc, GlcNAc, and ManNAc were prepared by either a one- or a two-step process. The anomeric selenides underwent facile C-Se homolysis to provide the correspondi

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