Cas 214335-84-9,(R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-1,3,3-trimethyl-cyclohexene

214335-84-9

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Basic information

Product Name: (R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-1,3,3-trimethyl-cyclohexene
Synonyms:
CAS NO:214335-84-9
Molecular Formula:
Molecular Weight: 398.777
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: (R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-1,3,3-trimethyl-cyclohexene(CAS DataBase Reference)
NIST Chemistry Reference: (R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-1,3,3-trimethyl-cyclohexene(214335-84-9)
EPA Substance Registry System: (R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-1,3,3-trimethyl-cyclohexene(214335-84-9)

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: 214335-84-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214335-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,3,3 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 214335-84:
(8*2)+(7*1)+(6*4)+(5*3)+(4*3)+(3*5)+(2*8)+(1*4)=109
109 % 10 = 9
So 214335-84-9 is a valid CAS Registry Number.

214335-84-9Upstream product

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214335-84-9Relevant academic research and scientific papers

Carotenoids and related polyenes. Part 5. Lewis acid-promoted stereoselective rearrangement of 5,6-epoxy carotenoid model compounds

Yamano, Yumiko,Tode, Chisato,Ito, Masayoshi

, p. 2569 - 2581 (2007/10/03)

The novel acyclic tetrasubstituted olefinic end group and the cyclopentyl end group of carotenoids were obtained by Lewis acid-promoted stereoselective rearrangement of the epoxide end group of 5,6-epoxy carotenoids. The scope and limitation of this rearr

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