Cas 220758-07-6,4-nitrophenyl 4-O-(2'-bromoprop-2'-enyl)-6-O-(tert-butyldimethylsilyl)-2,3-dideoxy-α-D-threo-hex-2-enopyranoside

220758-07-6

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Basic information

Product Name: 4-nitrophenyl 4-O-(2'-bromoprop-2'-enyl)-6-O-(tert-butyldimethylsilyl)-2,3-dideoxy-α-D-threo-hex-2-enopyranoside
Synonyms: 4-nitrophenyl 4-O-(2'-bromoprop-2'-enyl)-6-O-(tert-butyldimethylsilyl)-2,3-dideoxy-α-D-threo-hex-2-enopyranoside
CAS NO:220758-07-6
Molecular Formula:
Molecular Weight: 500.462
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: 4-nitrophenyl 4-O-(2'-bromoprop-2'-enyl)-6-O-(tert-butyldimethylsilyl)-2,3-dideoxy-α-D-threo-hex-2-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 4-nitrophenyl 4-O-(2'-bromoprop-2'-enyl)-6-O-(tert-butyldimethylsilyl)-2,3-dideoxy-α-D-threo-hex-2-enopyranoside(220758-07-6)
EPA Substance Registry System: 4-nitrophenyl 4-O-(2'-bromoprop-2'-enyl)-6-O-(tert-butyldimethylsilyl)-2,3-dideoxy-α-D-threo-hex-2-enopyranoside(220758-07-6)

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: 220758-07-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220758-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,7,5 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 220758-07:
(8*2)+(7*2)+(6*0)+(5*7)+(4*5)+(3*8)+(2*0)+(1*7)=116
116 % 10 = 6
So 220758-07-6 is a valid CAS Registry Number.

220758-07-6Upstream product

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220758-07-6Relevant academic research and scientific papers

Palladium-mediated cyclization on carbohydrate templates. 3. extension of the cyclization to the threo series

Bedjeguelal, Karim,Joseph, Laure,Bolitt, Veronique,Sinou, Denis

, p. 221 - 232 (2007/10/03)

The palladium(0)-catalyzed Heck-type cyclization-β-alkoxy elimination reaction leading to enantiopure bicyclic compounds in the case of erythro 2,3-unsaturated glycosides has been successfully extended to the threo stereoisomer by only changing the aglyco

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