2415-96-5 Usage
Uses
Used in Organic Synthesis:
2,2,3,3-Tetramethylcyclopropanemethanol serves as a fundamental building block in the realm of organic synthesis. Its structural features allow it to be a precursor for the preparation of a wide array of other organic compounds, making it an essential component in the synthesis of various chemical products.
Used in Solvent Applications:
In certain industries, 2,2,3,3-Tetramethylcyclopropanemethanol is utilized as a solvent. Its chemical properties make it suitable for dissolving a range of substances, which is crucial in processes that require the use of solvents to facilitate reactions or to extract specific components from mixtures.
Used in Pharmaceutical Industry:
2,2,3,3-Tetramethylcyclopropanemethanol is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity enable the creation of complex molecules that can be further developed into potential drug candidates, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
In the field of chemical research, 2,2,3,3-Tetramethylcyclopropanemethanol is employed as a model compound for studying the properties and reactions of cyclopropane derivatives. Its use in research helps to deepen the understanding of the underlying chemical mechanisms and to develop new synthetic strategies and methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 2415-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2415-96:
(6*2)+(5*4)+(4*1)+(3*5)+(2*9)+(1*6)=75
75 % 10 = 5
So 2415-96-5 is a valid CAS Registry Number.
2415-96-5Relevant academic research and scientific papers
Cyclopropanation of allylic alcohols using substituted haloalkylzinc reagents: Synthesis of gem-Dimethylcyclopropanes
Charette,Wilb
, p. 176 - 178 (2007/10/03)
gem-Dimethylcyclopropanes were obtained by a cyclopropanation of allylic alcohols and ethers using a mixture of diethylzinc and 2,2-diiodopropane in 53-96% yields. Enantioenriched gem-dimethylcyclopropanes were also synthesized using a glucose-derived aux
