Cas 211566-89-1,Biphenyl-4-carboxylic acid (1R,2S,3R,4S)-3-allyl-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopentyl ester

211566-89-1

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Basic information

Product Name: Biphenyl-4-carboxylic acid (1R,2S,3R,4S)-3-allyl-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopentyl ester
Synonyms: Biphenyl-4-carboxylic acid (1R,2S,3R,4S)-3-allyl-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopentyl ester
CAS NO:211566-89-1
Molecular Formula:
Molecular Weight: 705.097
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: Biphenyl-4-carboxylic acid (1R,2S,3R,4S)-3-allyl-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopentyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Biphenyl-4-carboxylic acid (1R,2S,3R,4S)-3-allyl-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopentyl ester(211566-89-1)
EPA Substance Registry System: Biphenyl-4-carboxylic acid (1R,2S,3R,4S)-3-allyl-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopentyl ester(211566-89-1)

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: 211566-89-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 211566-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,5,6 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 211566-89:
(8*2)+(7*1)+(6*1)+(5*5)+(4*6)+(3*6)+(2*8)+(1*9)=121
121 % 10 = 1
So 211566-89-1 is a valid CAS Registry Number.

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211566-89-1Relevant academic research and scientific papers

A short synthesis of optically active corey lactone by means of the dirhodium(II)-catalyzed intramolecular C-H insertion reaction of an α-diazo ketone

Yakura, Takayuki,Yamada, Seiji,Azuma, Miki,Ueki, Akiharu,Ikeda, Masazumi

, p. 973 - 974 (2007/10/03)

Optically active Corey lactone 8 has been synthesized using a dirhodium(II)-catalyzed intramolecular C-H insertion reaction of chiral α- diazo-β-oxo ester 2 as a key step.

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