Cas 910247-30-2,(R,3E,7E,11E)-benzyl 4,8,12-trimethylcyclotetradeca-3,7,11-trienecarboxylate

910247-30-2

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Basic information

Product Name: (R,3E,7E,11E)-benzyl 4,8,12-trimethylcyclotetradeca-3,7,11-trienecarboxylate
Synonyms: (R,3E,7E,11E)-benzyl 4,8,12-trimethylcyclotetradeca-3,7,11-trienecarboxylate
CAS NO:910247-30-2
Molecular Formula:
Molecular Weight: 366.544
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,3E,7E,11E)-benzyl 4,8,12-trimethylcyclotetradeca-3,7,11-trienecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R,3E,7E,11E)-benzyl 4,8,12-trimethylcyclotetradeca-3,7,11-trienecarboxylate(910247-30-2)
EPA Substance Registry System: (R,3E,7E,11E)-benzyl 4,8,12-trimethylcyclotetradeca-3,7,11-trienecarboxylate(910247-30-2)

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: 910247-30-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 910247-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,2,4 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 910247-30:
(8*9)+(7*1)+(6*0)+(5*2)+(4*4)+(3*7)+(2*3)+(1*0)=132
132 % 10 = 2
So 910247-30-2 is a valid CAS Registry Number.

910247-30-2Upstream product

100-51-6 benzyl alcohol

910247-30-2Downstream Products

53915-41-6 2-[(1R,3E,7E,11E)-4,8,12-trimethylcyclotetradeca-3,7,11-trien-1-yl]propan-2-ol

910247-30-2Relevant academic research and scientific papers

Enantioselective synthesis of α-terpineol and nephthenol by intramolecular acyloxazolidinone enolate alkylations

Jin, Yinghua,Coates, Robert M.

, p. 2902 - 2904 (2008/09/18)

Enolate anions generated from norterpenyl bromides bearing oxazolidinone chiral auxiliaries at the chain termini underwent efficient, stereo-biased cyclizations to form 6- and 14-membered rings in novel synthetic routes to α-terpineol and nephthenol enantiomers. The Royal Society of Chemistry 2006.

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