Cas 915221-87-3,6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-β-L-glycero-L-ido-nona-1,4-furanose

915221-87-3

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Basic information

Product Name: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-β-L-glycero-L-ido-nona-1,4-furanose
Synonyms: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-β-L-glycero-L-ido-nona-1,4-furanose
CAS NO:915221-87-3
Molecular Formula:
Molecular Weight: 483.565
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: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-β-L-glycero-L-ido-nona-1,4-furanose(CAS DataBase Reference)
NIST Chemistry Reference: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-β-L-glycero-L-ido-nona-1,4-furanose(915221-87-3)
EPA Substance Registry System: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-β-L-glycero-L-ido-nona-1,4-furanose(915221-87-3)

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: 915221-87-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915221-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,2,2 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 915221-87:
(8*9)+(7*1)+(6*5)+(5*2)+(4*2)+(3*1)+(2*8)+(1*7)=153
153 % 10 = 3
So 915221-87-3 is a valid CAS Registry Number.

915221-87-3Upstream product

915221-85-1 3,9-di-O-benzyl-1,2-O-isopropylidene-7,8-dideoxy-5,6-oxirano-α-D-glycero-L-ido-nona-1,4-furanose

915221-87-3Downstream Products

915221-87-3Relevant academic research and scientific papers

Polyhydroxylated homoazepanes and 1-deoxy-homonojirimycin analogues: Synthesis and glycosidase inhibition study

Markad, Shankar D.,Karanjule, Narayan S.,Sharma, Tarun,Sabharwal, Sushma G.,Dhavale, Dilip D.

, p. 3675 - 3680 (2006)

The Johnson-Claisen rearrangement of d-gluco and l-ido-derived allylic orthoesters afforded γ,δ-unsaturated ester that on ester reduction, epoxidation, regioselective oxirane opening by sodium azide and hydrogenation led to sugar amino alcohols - immediat

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