Cas 1454577-96-8,(1(1’)E)-1-deoxy-1-(dibenzyloxyphosphoryl)methylidene-2,3,5-tri-O-tert-butyldimethylsilyl-D-ribofuranose

1454577-96-8

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Basic information

Product Name: (1(1’)E)-1-deoxy-1-(dibenzyloxyphosphoryl)methylidene-2,3,5-tri-O-tert-butyldimethylsilyl-D-ribofuranose
Synonyms: (1(1’)E)-1-deoxy-1-(dibenzyloxyphosphoryl)methylidene-2,3,5-tri-O-tert-butyldimethylsilyl-D-ribofuranose
CAS NO:1454577-96-8
Molecular Formula:
Molecular Weight: 749.16
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(1’)E)-1-deoxy-1-(dibenzyloxyphosphoryl)methylidene-2,3,5-tri-O-tert-butyldimethylsilyl-D-ribofuranose(CAS DataBase Reference)
NIST Chemistry Reference: (1(1’)E)-1-deoxy-1-(dibenzyloxyphosphoryl)methylidene-2,3,5-tri-O-tert-butyldimethylsilyl-D-ribofuranose(1454577-96-8)
EPA Substance Registry System: (1(1’)E)-1-deoxy-1-(dibenzyloxyphosphoryl)methylidene-2,3,5-tri-O-tert-butyldimethylsilyl-D-ribofuranose(1454577-96-8)

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: 1454577-96-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1454577-96-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,5,7 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1454577-96:
(9*1)+(8*4)+(7*5)+(6*4)+(5*5)+(4*7)+(3*7)+(2*9)+(1*6)=198
198 % 10 = 8
So 1454577-96-8 is a valid CAS Registry Number.

1454577-96-8Upstream product

1454577-94-6 (1(1’)Z)-1-deoxy-1-(dibenzyloxyphosphoryl)methylidene-2,3,5-tri-O-tert-butyldimethylsilyl-D-ribofuranose

1454577-96-8Downstream Products

1454577-96-8Relevant academic research and scientific papers

A novel base-induced isomerization gives access to unprecedented (E)-exo-glycals

Eppe, Guillaume,Dumitrescu, Lidia,Pierrot, Olivier,Li, Tianlei,Pan, Weidong,Vincent, Stephane P.

, p. 11547 - 11552 (2013)

Bump the base: This study reports the discovery of the base-induced Z-to-E isomerization of exo-glycals bearing an electron-withdrawing group (EWG). The scope of this novel transformation regarding the carbohydrate unit is also discussed. After elucidating the mechanism, preparation of novel (E)-exo- glycals was performed (TBS=tert-butyldimethylsilyl). Copyright

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