4070-14-8 Usage
Uses
Used in Organic Synthesis:
2,2,3,3-Tetramethylcyclobutanone is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic molecules, facilitating the creation of a wide range of chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,2,3,3-Tetramethylcyclobutanone is utilized as a key intermediate in the synthesis of various medicinal compounds, playing a crucial role in drug development due to its reactive ketone group and unique structural features.
Used in Fragrance Industry:
2,2,3,3-Tetramethylcyclobutanone is employed as a fragrance ingredient, capitalizing on its slightly minty odor to enhance the scent profiles of different perfumes and scented products.
Used in Food Industry:
As a flavoring agent, 2,2,3,3-Tetramethylcyclobutanone is used in the food industry to impart or modify flavors in various food products, taking advantage of its distinctive minty aroma.
Used in Material Development:
2,2,3,3-Tetramethylcyclobutanone has been studied for its potential in the development of new materials, suggesting its use as a component in innovative material sciences for future applications.
Used as a Solvent in Chemical Processes:
In various chemical processes, 2,2,3,3-Tetramethylcyclobutanone serves as a solvent, leveraging its solubility properties to dissolve other substances and facilitate chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 4070-14-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4070-14:
(6*4)+(5*0)+(4*7)+(3*0)+(2*1)+(1*4)=58
58 % 10 = 8
So 4070-14-8 is a valid CAS Registry Number.
4070-14-8Relevant academic research and scientific papers
Titanium(IV) chloride-mediated ring cleavage and Michael addition of 3,3-dialkylcyclobutanones and 3-[(trimethylsilyl)methyl]-cyclobutanones
Okuno, Ryosuke,Matsuo, Jun-Ichi,Ishibashi, Hiroyuki
experimental part, p. 793 - 797 (2012/08/07)
β′-Chloro and β′,γ′-unsaturated trichlorotitanium enolates, which were formed in situ by titanium(IV) chloride-mediated ring cleavage of 3,3-dialkylcyclobutanones and 3-[(trimethylsilyl)methyl]cyclobutanones, reacted with enones to give Michael adducts wi
Synthesis of [1.1.1]Propellanes by Cyclization of 3-Alkylidenecyclobutylidenes
Kenndoff, Monika,Singer, Andrea,Szeimies, Guenter
, p. 217 - 232 (2007/10/03)
Starting from tricyclo[3.1.0.02,6]hexane 5 and 1-bromobicyclo[1.1.0]butane 6, a series of [1.1.1]propellanes 15 and 21 has been synthesized which carry alkyl, aryl, alkenyl, and alkynyl groups. Propellane formation proceeded via 1-bromo-1-chlor
