Cas 1087192-40-2,(1R,2S,5R)-2-tert-butyldimethylsilanyloxy-5-trityloxymethylcyclopentanol

1087192-40-2

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Basic information

Product Name: (1R,2S,5R)-2-tert-butyldimethylsilanyloxy-5-trityloxymethylcyclopentanol
Synonyms: (1R,2S,5R)-2-tert-butyldimethylsilanyloxy-5-trityloxymethylcyclopentanol
CAS NO:1087192-40-2
Molecular Formula:
Molecular Weight: 488.742
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: (1R,2S,5R)-2-tert-butyldimethylsilanyloxy-5-trityloxymethylcyclopentanol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,5R)-2-tert-butyldimethylsilanyloxy-5-trityloxymethylcyclopentanol(1087192-40-2)
EPA Substance Registry System: (1R,2S,5R)-2-tert-butyldimethylsilanyloxy-5-trityloxymethylcyclopentanol(1087192-40-2)

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: 1087192-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1087192-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,7,1,9 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1087192-40:
(9*1)+(8*0)+(7*8)+(6*7)+(5*1)+(4*9)+(3*2)+(2*4)+(1*0)=162
162 % 10 = 2
So 1087192-40-2 is a valid CAS Registry Number.

1087192-40-2Upstream product

870294-70-5 (2R,3R,4S)-[3-benzyloxy-4-(tert-butyldimethylsilyloxy)-2-trityloxymethyl]cyclopentan-1-one-1,3-propanedithioketal

1087192-40-2Downstream Products

1087192-40-2Relevant academic research and scientific papers

A linchpin carbacyclization approach for the synthesis of carbanucleosides

Leung, Leo M. H.,Gibson, Vicky,Linclau, Bruno

experimental part, p. 9197 - 9206 (2009/04/06)

(Chemical Equation Presented) A convenient synthesis of carbanucleosides, with both enantiomers equally accessible, is reported. The key step is a tandem linchpin cyclization process to give access to substituted carbafuranose derivatives having the corre

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