Cas 960238-01-1,(E)-ethyl 3-O-benzyl-1,2-O-isopropylidene-5-[benzyl(benzyloxycarbonyl)amino]-5,6,7-trideoxy-β-L-ido-6-eno-octafuranuronate

960238-01-1

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Basic information

Product Name: (E)-ethyl 3-O-benzyl-1,2-O-isopropylidene-5-[benzyl(benzyloxycarbonyl)amino]-5,6,7-trideoxy-β-L-ido-6-eno-octafuranuronate
Synonyms: (E)-ethyl 3-O-benzyl-1,2-O-isopropylidene-5-[benzyl(benzyloxycarbonyl)amino]-5,6,7-trideoxy-β-L-ido-6-eno-octafuranuronate
CAS NO:960238-01-1
Molecular Formula:
Molecular Weight: 601.697
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: (E)-ethyl 3-O-benzyl-1,2-O-isopropylidene-5-[benzyl(benzyloxycarbonyl)amino]-5,6,7-trideoxy-β-L-ido-6-eno-octafuranuronate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-ethyl 3-O-benzyl-1,2-O-isopropylidene-5-[benzyl(benzyloxycarbonyl)amino]-5,6,7-trideoxy-β-L-ido-6-eno-octafuranuronate(960238-01-1)
EPA Substance Registry System: (E)-ethyl 3-O-benzyl-1,2-O-isopropylidene-5-[benzyl(benzyloxycarbonyl)amino]-5,6,7-trideoxy-β-L-ido-6-eno-octafuranuronate(960238-01-1)

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: 960238-01-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960238-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,2,3 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 960238-01:
(8*9)+(7*6)+(6*0)+(5*2)+(4*3)+(3*8)+(2*0)+(1*1)=161
161 % 10 = 1
So 960238-01-1 is a valid CAS Registry Number.

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960238-01-1Relevant academic research and scientific papers

Synthesis and glycosidase inhibitory studies of pentahydroxyindolizidines: D-glucose-derived aziridine-2-carboxylate approach

Kumar, K.S. Ajish,Chaudhari, Vinod D.,Puranik, Vedavati G.,Dhavale, Dilip D.

, p. 4895 - 4901 (2007)

D-Glucose-derived aziridine-2-carboxylate 1 was converted into α-amino aldehyde 7, which, after Wittig olefination, asymmetric dihydroxylation, hydrogenation followed by LiAlH4 reduction, and N-Cbz protection, afforded two diastereomeric pyrrol

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