Cas 1256092-82-6,(Z)-ethyl 2-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-glucopyranosyl)-3-aminobut-2-enoate

1256092-82-6

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Basic information

Product Name: (Z)-ethyl 2-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-glucopyranosyl)-3-aminobut-2-enoate
Synonyms:
CAS NO:1256092-82-6
Molecular Formula:
Molecular Weight: 590.673
EINECS: N/A
Product Categories: N/A
Mol File: 1256092-82-6.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: (Z)-ethyl 2-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-glucopyranosyl)-3-aminobut-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-ethyl 2-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-glucopyranosyl)-3-aminobut-2-enoate(1256092-82-6)
EPA Substance Registry System: (Z)-ethyl 2-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-glucopyranosyl)-3-aminobut-2-enoate(1256092-82-6)

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: 1256092-82-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256092-82-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,0,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1256092-82:
(9*1)+(8*2)+(7*5)+(6*6)+(5*0)+(4*9)+(3*2)+(2*8)+(1*2)=156
156 % 10 = 6
So 1256092-82-6 is a valid CAS Registry Number.

1256092-82-6Upstream product

1256092-82-6Downstream Products

1256092-82-6Relevant articles and documents

Solvent-free and stereoselective synthesis of C-glycosides by michael-type addition of enamino esters to 2-nitro- d -glucal

Zhang, Ti,Yu, Chu-Yi,Huang, Zhi-Tang,Jia, Yue-Mei

supporting information; experimental part, p. 2174 - 2178 (2010/10/21)

Michael-type addition of enamino esters to 3,4,6-tri-O-benzyl-2-nitro-d- glucal under solvent-free conditions formed C-glycosides in excellent yields with high stereoselectivity. Reduction of the nitro group afforded the corresponding bicyclic 2-amino C-g

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