Cas 915221-86-2,6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-α-D-glycero-D-gluco-nona-1,4-furanose

915221-86-2

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Basic information

Product Name: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-α-D-glycero-D-gluco-nona-1,4-furanose
Synonyms: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-α-D-glycero-D-gluco-nona-1,4-furanose
CAS NO:915221-86-2
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-α-D-glycero-D-gluco-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-α-D-glycero-D-gluco-nona-1,4-furanose(915221-86-2)
EPA Substance Registry System: 6-azido-3,9-di-O-benzyl-1,2-O-isopropylidene-6,7,8-trideoxy-α-D-glycero-D-gluco-nona-1,4-furanose(915221-86-2)

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: 915221-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915221-86-2 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 915221-86:
(8*9)+(7*1)+(6*5)+(5*2)+(4*2)+(3*1)+(2*8)+(1*6)=152
152 % 10 = 2
So 915221-86-2 is a valid CAS Registry Number.

915221-86-2Upstream product

915221-84-0 3,9-di-O-benzyl-1,2-O-isopropylidene-7,8-dideoxy-5,6-oxirano-β-L-glycero-D-gluco-nona-1,4-furanose

915221-86-2Downstream Products

915221-86-2Relevant 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 (2008/10/09)

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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