Cas 5111-14-8,1,2-O-isopropylidene-5-O-benzyl-3-hydroxy-α-D-glucofuranosiduronamide

5111-14-8

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Basic information

Product Name: 1,2-O-isopropylidene-5-O-benzyl-3-hydroxy-α-D-glucofuranosiduronamide
Synonyms: 1,2-O-isopropylidene-5-O-benzyl-3-hydroxy-α-D-glucofuranosiduronamide
CAS NO:5111-14-8
Molecular Formula:
Molecular Weight: 323.346
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: 1,2-O-isopropylidene-5-O-benzyl-3-hydroxy-α-D-glucofuranosiduronamide(CAS DataBase Reference)
NIST Chemistry Reference: 1,2-O-isopropylidene-5-O-benzyl-3-hydroxy-α-D-glucofuranosiduronamide(5111-14-8)
EPA Substance Registry System: 1,2-O-isopropylidene-5-O-benzyl-3-hydroxy-α-D-glucofuranosiduronamide(5111-14-8)

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: 5111-14-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 5111-14-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5111-14:
(6*5)+(5*1)+(4*1)+(3*1)+(2*1)+(1*4)=48
48 % 10 = 8
So 5111-14-8 is a valid CAS Registry Number.

5111-14-8Upstream product

5111-14-8Downstream Products

222425-25-4 1,2-O-isopropylidene-5-O-benzyl-3-O-phenoxycarbonyl-α-D-glucofuranosiduronamide

5111-14-8Relevant academic research and scientific papers

Acceptor site recognition of transglycosylase inhibitors A β-D- glucopyranosyl-(1 → 2)-α-D-glucopyranuronamide-derived moenomycin analogue

Ferse, Falk-Thilo,Floeder, Kerstin,Hennig, Lothar,Findeisen, Matthias,Welzel, Peter,Mueller, Dietrich,Van Heijenoort, Jean

, p. 3749 - 3766 (2007/10/03)

The synthesis, the antibiotic and the transglycosylase inhibiting properties of a disaccharide analogue of moenomycin A in which the NHAc group of unit E is replaced by a hydroxyl function are described. It can be concluded that this NHAc group is essenti

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