102616-12-6 Usage
General Description
The chemical (2R,3R,4E)-2-(benzyloxy)-3,7-dimethyloct-4-enal, also known as benzyloxy aldehyde, is a compound with a molecular formula of C16H24O2. It is a colorless to pale yellow liquid with a strong, sweet, floral aroma. (2R,3R,4E)-2-(benzyloxy)-3,7-dimethyloct-4-enal is often used as a fragrance ingredient and is found in natural sources such as flowers and essential oils. It is also used in the production of perfumes, soaps, and other cosmetic products. Additionally, benzyloxy aldehyde has potential applications in the food industry, as it is used to create flavorings and enhance the aroma of food products.
Check Digit Verification of cas no
The CAS Registry Mumber 102616-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102616-12:
(8*1)+(7*0)+(6*2)+(5*6)+(4*1)+(3*6)+(2*1)+(1*2)=76
76 % 10 = 6
So 102616-12-6 is a valid CAS Registry Number.
102616-12-6Relevant articles and documents
Stereocontrolled Synthesis of Highly Oxygenated Acyclic Systems via the Enolate Claisen Rearrangement of O-Protected Allylic Glycolates
Gould, Thomas J.,Balestra, Michael,Wittman, Mark D.,Gary, Jill A.,Rossano, Lucius T.,Kallmerten, James
, p. 3889 - 3901 (2007/10/02)
Enolate Claisen rearrangement of E- and Z-allylic glycolates yields the syn- and anti-2-alkoxy-3-alkyl 4-enoates, respectively, in good yields (60-90percent) and with high internal diastereoselectivity.Incorporation of the glycolate Claisen procedure into an iterative sequence consisting of Claisen rearrangement and homologation by addition of vinyl nucleophiles results in the efficient, stereocontrolled generation of remotely functionalized, highly oxygenated acyclic systems.This strategy is demonstrated in stereoselective syntheses of pine sawfly pheromone 42 and tocopherol side-chain intermediate 30.