Cas 848349-93-9,1,6-anhydro-2-O-benzyl-3,4-dideoxy-3,4-(N-o-nitrobenzenesulfonylepimino)-β-D-allopyranose

848349-93-9

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Basic information

Product Name: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-3,4-(N-o-nitrobenzenesulfonylepimino)-β-D-allopyranose
Synonyms: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-3,4-(N-o-nitrobenzenesulfonylepimino)-β-D-allopyranose
CAS NO:848349-93-9
Molecular Formula:
Molecular Weight: 418.427
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: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-3,4-(N-o-nitrobenzenesulfonylepimino)-β-D-allopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-3,4-(N-o-nitrobenzenesulfonylepimino)-β-D-allopyranose(848349-93-9)
EPA Substance Registry System: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-3,4-(N-o-nitrobenzenesulfonylepimino)-β-D-allopyranose(848349-93-9)

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: 848349-93-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 848349-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,3,4 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 848349-93:
(8*8)+(7*4)+(6*8)+(5*3)+(4*4)+(3*9)+(2*9)+(1*3)=219
219 % 10 = 9
So 848349-93-9 is a valid CAS Registry Number.

848349-93-9Upstream product

359772-43-3 1,6-Anhydro-4-azido-2-O-benzyl-4-deoxy-3-O-tosyl-β-D-glucopyranose

848349-93-9Downstream Products

848349-93-9Relevant academic research and scientific papers

Preparation of N-nosyl-3,4-epimines derived from levoglucosan by sodium borohydride reduction

Kroutil, Jiri,Karban, Jindrich

, p. 503 - 506 (2007/10/03)

Starting from 1,6-anhydro-β-d-glucopyranose 1 (levoglucosan), N-o-nitrobenzenesulfonyl (nosyl) 3,4-epimino derivatives with d-allo, d-galacto, and d-talo configurations have been prepared via NaBH4 reduction of suitably substituted azido tosylates. The benefits and limitations of this method over the classical LiAlH4 reduction method are discussed.

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