1042150-18-4 Usage
Description
(R)-methyl 3-(4-methyl-6-oxocyclohex-1-enyl)propanoate is a chemical compound characterized by its molecular formula C12H18O3. It is a methyl ester derivative of 3-(4-methyl-6-oxocyclohex-1-enyl)propanoic acid, known for its sweet, fruity, and floral odor.
Uses
Used in Flavor and Fragrance Industry:
(R)-methyl 3-(4-methyl-6-oxocyclohex-1-enyl)propanoate is used as a flavoring agent and fragrance ingredient for its distinctive sweet, fruity, and floral scent. This makes it an ideal additive for the creation of various cosmetics, perfumes, and food products, enhancing their sensory appeal and consumer experience.
Used in Pharmaceutical and Agrochemical Research:
Beyond its olfactory applications, (R)-methyl 3-(4-methyl-6-oxocyclohex-1-enyl)propanoate also exhibits potential bioactive properties. This characteristic positions it as a valuable compound for research and development within the pharmaceutical and agrochemical industries, where it may be explored for its possible therapeutic or pesticidal applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1042150-18-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,1,5 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1042150-18:
(9*1)+(8*0)+(7*4)+(6*2)+(5*1)+(4*5)+(3*0)+(2*1)+(1*8)=84
84 % 10 = 4
So 1042150-18-4 is a valid CAS Registry Number.
1042150-18-4Relevant articles and documents
Asymmetric Total Synthesis of (-)-Lycospidine A
Xu, Shiyan,Zhang, Jing,Ma, Donghui,Xu, Dengyu,Xie, Xingang,She, Xuegong
, p. 4682 - 4685 (2016)
The first asymmetric total synthesis of the structurally unique Lycopodium alkaloid (-)-lycospidine A, containing an unprecedented five-membered ring, has been accomplished in only 10 steps with 21.6% overall yield from the known conveniently available sulfoxide. This protecting-group-free short synthesis relied on the use of a key amidation/aza-Prins domino cyclization reaction to rapidly construct the tricyclic skeleton and two continuous stereocenters (one of which is a bridged quaternary stereocenter). An intramolecular aldol condensation was successfully utilized to establish the unique five-membered ring, and a late-stage oxidation inspired by biosynthesis pathway was adopted to synthesize the diosphenol ring of (-)-lycospidine A.
