65108-31-8 Usage
Uses
Used in Pharmaceutical Industry:
2,2-diMethylbut-3-yn-1-ol is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure, which allows for the creation of a wide range of medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2,2-diMethylbut-3-yn-1-ol is used as a precursor in the production of various agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used in Fragrance Industry:
2,2-diMethylbut-3-yn-1-ol is utilized as a building block in the synthesis of fragrances, providing unique scents and enhancing the overall aroma of various products.
Used as a Solvent:
Due to its solvent properties, 2,2-diMethylbut-3-yn-1-ol is used in various applications where a solvent is required, such as in the manufacturing process of certain chemicals and materials.
Used in Plastics and Rubber Production:
2,2-diMethylbut-3-yn-1-ol serves as a raw material in the production of plastics and rubber, contributing to the development of new materials with specific properties and applications.
Safety Precautions:
As a potentially hazardous substance, proper handling and storage of 2,2-diMethylbut-3-yn-1-ol are essential to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 65108-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,0 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65108-31:
(7*6)+(6*5)+(5*1)+(4*0)+(3*8)+(2*3)+(1*1)=108
108 % 10 = 8
So 65108-31-8 is a valid CAS Registry Number.
65108-31-8Relevant academic research and scientific papers
Enantioselective Construction of Tertiary Fluoride Stereocenters by Organocatalytic Fluorocyclization
Biosca, Maria,Eriksson, Lars,Hedberg, Martin,Himo, Fahmi,Lübcke, Marvin,Szabó, Kálmán J.,Wang, Qiang
, p. 20048 - 20057 (2020/11/27)
1,1-Disubstituted styrenes with internal oxygen and nitrogen nucleophiles undergo oxidative fluorocyclization reactions with in situ generated chiral iodine(III)-catalysts. The resulting fluorinated tetrahydrofurans and pyrrolidines contain a tertiary carbon-fluorine stereocenter. Application of a new 1-naphthyllactic acid-based iodine(III)-catalyst allows the control of tertiary carbon-fluorine stereocenters with up to 96% ee. Density functional theory calculations are performed to investigate the details of the mechanism and the factors governing the stereoselectivity of the reaction.
