Cas 851626-45-4,(2RS,1'S,2'E) 2-(4-methoxybenzyloxy)hex-5-enoic acid 4'-(tert-butyl(diphenyl)silyloxy)-1',3'-dimethylbut-2'-enyl ester

851626-45-4

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Basic information

Product Name: (2RS,1'S,2'E) 2-(4-methoxybenzyloxy)hex-5-enoic acid 4'-(tert-butyl(diphenyl)silyloxy)-1',3'-dimethylbut-2'-enyl ester
Synonyms: (2RS,1'S,2'E) 2-(4-methoxybenzyloxy)hex-5-enoic acid 4'-(tert-butyl(diphenyl)silyloxy)-1',3'-dimethylbut-2'-enyl ester
CAS NO:851626-45-4
Molecular Formula:
Molecular Weight: 586.844
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: (2RS,1'S,2'E) 2-(4-methoxybenzyloxy)hex-5-enoic acid 4'-(tert-butyl(diphenyl)silyloxy)-1',3'-dimethylbut-2'-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2RS,1'S,2'E) 2-(4-methoxybenzyloxy)hex-5-enoic acid 4'-(tert-butyl(diphenyl)silyloxy)-1',3'-dimethylbut-2'-enyl ester(851626-45-4)
EPA Substance Registry System: (2RS,1'S,2'E) 2-(4-methoxybenzyloxy)hex-5-enoic acid 4'-(tert-butyl(diphenyl)silyloxy)-1',3'-dimethylbut-2'-enyl ester(851626-45-4)

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: 851626-45-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 851626-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,6,2 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 851626-45:
(8*8)+(7*5)+(6*1)+(5*6)+(4*2)+(3*6)+(2*4)+(1*5)=174
174 % 10 = 4
So 851626-45-4 is a valid CAS Registry Number.

851626-45-4Upstream product

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851626-45-4Relevant academic research and scientific papers

Highly enantioselective sequential Claisen-Ireland/metathesis: Synthesis of cycloalkenes bearing two contiguous highly functionalized asymmetric centres

Francais, Antoine,Bedel, Olivier,Picoul, Willy,Meddour, Abdelkrim,Courtieu, Jacques,Haudrechy, Arnaud

, p. 1141 - 1155 (2007/10/03)

A sequence of two reactions, consisting of a highly stereoselective silylated ketene acetal Claisen-Ireland rearrangement followed by a ring closing metathesis, gave a stereocontrolled access to various carbocycles.

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