52505-39-2 Usage
Uses
Used in Organic Synthesis:
Diprop-2-enyl 2-benzylidenepropanedioate is used as a reagent in organic synthesis for the production of various organic compounds.
Used in Flavoring Agents:
Diprop-2-enyl 2-benzylidenepropanedioate is used as a flavoring agent in food and beverages, providing a fruity taste.
Used in Perfume and Fragrance Production:
Diprop-2-enyl 2-benzylidenepropanedioate is used in the production of perfumes and fragrances, contributing to their fruity scent.
Used in Pharmaceutical Industry:
Diprop-2-enyl 2-benzylidenepropanedioate has potential applications in the pharmaceutical industry, although specific uses are not detailed in the provided materials.
Used in Agrochemical Industry:
Diprop-2-enyl 2-benzylidenepropanedioate also has potential applications in the agrochemical industry, but the specific uses are not provided in the materials.
Safety Precautions:
It is important to handle Diprop-2-enyl 2-benzylidenepropanedioate with caution and adhere to safety protocols, as it may pose health risks if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 52505-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,0 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52505-39:
(7*5)+(6*2)+(5*5)+(4*0)+(3*5)+(2*3)+(1*9)=102
102 % 10 = 2
So 52505-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O4/c1-3-10-19-15(17)14(16(18)20-11-4-2)12-13-8-6-5-7-9-13/h3-9,12H,1-2,10-11H2
52505-39-2Relevant academic research and scientific papers
Asymmetric total synthesis of (-)-plicatic acid via a highly enantioselective and diastereoselective nucleophilic epoxidation of acyclic trisubstitued olefins
Sun, Bing-Feng,Hong, Ran,Kang, Yan-Biao,Deng, Li
supporting information; experimental part, p. 10384 - 10385 (2009/12/23)
(Chemical Equation Presented) The first total synthesis of (-)-plicatic acid has been achieved by a concise and enantioselective route. In this synthesis, a conceptually new strategy featuring an asymmetric epoxidation-intramolecular epoxy-ring-opening Friedel-Crafts reaction sequence was developed for the stereoselective construction of the 2,7′- cyclolignane skeleton bearing contiguous quaternary-quaternary-tertiary stereocenters. The implementation of this strategy was enabled by the development of a modified protocol for the Seebach epoxidation with TADOOH, which affords an unprecedented, highly enantioselective and diastereoselective epoxidation with a range of α-carbonyl-β-substituted acrylates 3.
