Cas 111192-14-4,methyl 2,3,4-tri-O-benzyl-6-O-<methyl (5-acetamido-4,7,8,9-tetra-O-acetyl-5-deoxy-3-O-<phenoxy(thiocarbonyl)>-β-D-erythro-L-gluco-2-nonulopyranosyl)onate>-α-D-glucopyranoside

111192-14-4

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Basic information

Product Name: methyl 2,3,4-tri-O-benzyl-6-O--β-D-erythro-L-gluco-2-nonulopyranosyl)onate>-α-D-glucopyranoside
Synonyms: methyl 2,3,4-tri-O-benzyl-6-O--β-D-erythro-L-gluco-2-nonulopyranosyl)onate>-α-D-glucopyranoside
CAS NO:111192-14-4
Molecular Formula:
Molecular Weight: 1090.17
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 2,3,4-tri-O-benzyl-6-O--β-D-erythro-L-gluco-2-nonulopyranosyl)onate>-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,3,4-tri-O-benzyl-6-O--β-D-erythro-L-gluco-2-nonulopyranosyl)onate>-α-D-glucopyranoside(111192-14-4)
EPA Substance Registry System: methyl 2,3,4-tri-O-benzyl-6-O--β-D-erythro-L-gluco-2-nonulopyranosyl)onate>-α-D-glucopyranoside(111192-14-4)

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: 111192-14-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 111192-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,9 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111192-14:
(8*1)+(7*1)+(6*1)+(5*1)+(4*9)+(3*2)+(2*1)+(1*4)=74
74 % 10 = 4
So 111192-14-4 is a valid CAS Registry Number.

111192-14-4Upstream product

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111192-14-4Relevant academic research and scientific papers

Glycosylation of 4,7,8,9-Tetra-O-acetyl-2-deoxy-2β,3β-epoxy-N-acetylneuraminic Acid Methyl Ester

Okamoto, Kaoru,Kondo, Tadao,Goto, Toshio

, p. 637 - 644 (2007/10/02)

Reaction of the 2β,3β-epoxyneuraminic acid derivative prepared from 2,3-dehydroneuraminic acid derivative with primary or secondary alcohol gave the corresponding glycoside(s) or ortho ester.

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