4057-31-2 Usage
Description
(1,3,3-trimethylnorbornan-2-yl) acetate, also known as exo-2-acetoxy-1,3,3-trimethylnorbornane, is a chemical compound with the molecular formula C12H20O2. It is a derivative of norbornane, a bicyclic hydrocarbon, and acetate, a functional group derived from acetic acid. (1,3,3-trimethylnorbornan-2-yl) acetate is characterized by its unique chemical structure and properties, making it a valuable and versatile compound in various fields of chemistry and industry.
Uses
Used in Flavor and Fragrance Industry:
(1,3,3-trimethylnorbornan-2-yl) acetate is used as a flavoring agent and fragrance ingredient for its pleasant, fruity odor. It is commonly incorporated into perfumes, colognes, and other scented products to enhance their aroma and appeal to consumers.
Used in Pharmaceutical Industry:
Due to its unique chemical structure and properties, (1,3,3-trimethylnorbornan-2-yl) acetate has potential applications in the pharmaceutical industry. It may be utilized in the development of new drugs or as an intermediate in the synthesis of pharmaceutical compounds.
Used in Agrochemical Industry:
(1,3,3-trimethylnorbornan-2-yl) acetate also has potential applications in the agrochemical industry. It may be used in the development of new agrochemical products or as an intermediate in the synthesis of agrochemical compounds, contributing to advancements in agriculture and pest control.
Check Digit Verification of cas no
The CAS Registry Mumber 4057-31-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,5 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4057-31:
(6*4)+(5*0)+(4*5)+(3*7)+(2*3)+(1*1)=72
72 % 10 = 2
So 4057-31-2 is a valid CAS Registry Number.
4057-31-2Relevant articles and documents
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-endo-ol in Nucleophilic Substitution Reactions
Koval'skaya,Kozlov
, p. 1925 - 1927 (2007/10/03)
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-endo-ol (fenchol) reacts with acetonitrile in the presence of sulfuric acid to selectively form an isofenchane derivative - N-acetyl-1,5,5-trimethylbicyclo[2.2.1]heptan-2-exo-amine as a result of nucleophilic addition at the most accessible carbon atom of a nonclassical 1,3,3-trimethylbicyclo[2.2.1]heptyl cation. The H2SO4-catalyzed reaction with acetic acid results in exclusive formation of 1,3,3-trimethylbicyclo[2.2.1]hept-2-exo-yl acetate, implying an SN2 reaction mechanism.
