Cas 92126-41-5,(R)-1-cyclohexyl-2-<(tert-butyldimethylsilyl)oxy>ethyl (E,E,E)-12-methyltrideca-2,8,10-trienoate

92126-41-5

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Basic information

Product Name: (R)-1-cyclohexyl-2-<(tert-butyldimethylsilyl)oxy>ethyl (E,E,E)-12-methyltrideca-2,8,10-trienoate
Synonyms: (R)-1-cyclohexyl-2-<(tert-butyldimethylsilyl)oxy>ethyl (E,E,E)-12-methyltrideca-2,8,10-trienoate
CAS NO:92126-41-5
Molecular Formula:
Molecular Weight: 462.789
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)-1-cyclohexyl-2-<(tert-butyldimethylsilyl)oxy>ethyl (E,E,E)-12-methyltrideca-2,8,10-trienoate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1-cyclohexyl-2-<(tert-butyldimethylsilyl)oxy>ethyl (E,E,E)-12-methyltrideca-2,8,10-trienoate(92126-41-5)
EPA Substance Registry System: (R)-1-cyclohexyl-2-<(tert-butyldimethylsilyl)oxy>ethyl (E,E,E)-12-methyltrideca-2,8,10-trienoate(92126-41-5)

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: 92126-41-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 92126-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92126-41:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*4)+(1*1)=115
115 % 10 = 5
So 92126-41-5 is a valid CAS Registry Number.

92126-41-5Upstream product

92126-41-5Downstream Products

92126-42-6 (2E,8E,10E)-12-Methyl-trideca-2,8,10-trienoic acid 1-cyclohexyl-2-hydroxy-ethyl ester

92126-41-5Relevant academic research and scientific papers

Hydrofluoric Acid Catalyzed Intramolecular Diels-Alder Reactions

Roush, William R.,Gillis, Herbert R.,Essenfeld, Amy P.

, p. 4674 - 4682 (2007/10/02)

Studies of catalysis of intramolecular Diels-Alder reactions of trienes activated with substituted 2-hydroxyethyl esters are described.Triene esters 1, 11, 22, and 26 cyclize in moderate to good yield (44-78percent) when exposed to aqueous HF in acetonitr

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