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Ethanone, 1-(2,2,3,3-tetramethylcyclopropyl)is a unique chemical compound that features a cyclopropyl ring with four methyl substitutions. It is a member of the ketone family, known for its versatile applications in organic synthesis and as a solvent in a range of chemical reactions. The presence of the 2,2,3,3-tetramethylcyclopropyl group endows the molecule with steric hindrance, enhancing its stability against enzymatic degradation and making it suitable for various environments. Ethanone, 1-(2,2,3,3-tetramethylcyclopropyl)holds promise for use in chemistry, pharmaceuticals, and materials science due to its structural properties and reactivity.

60802-86-0

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60802-86-0 Usage

Uses

Used in Organic Synthesis:
Ethanone, 1-(2,2,3,3-tetramethylcyclopropyl)is utilized as a key intermediate in organic synthesis for the creation of complex molecules and pharmaceuticals. Its unique structure allows for the development of new compounds with specific properties, making it a valuable component in the synthesis of novel drugs and other chemical products.
Used in Chemical Reactions as a Solvent:
Ethanone, 1-(2,2,3,3-tetramethylcyclopropyl)serves as an effective solvent in various chemical reactions, facilitating processes that require a stable and reactive medium. Its resistance to degradation and compatibility with a wide range of substances make it an ideal choice for solvent applications in the chemical industry.
Used in Pharmaceutical Development:
Ethanone, 1-(2,2,3,3-tetramethylcyclopropyl)is employed in the pharmaceutical industry for the development of new drugs. Its steric hindrance and stability contribute to the creation of molecules with enhanced properties, such as improved bioavailability and targeted delivery, which are crucial for the effectiveness of pharmaceutical agents.
Used in Materials Science:
In the field of materials science, Ethanone, 1-(2,2,3,3-tetramethylcyclopropyl)- is explored for its potential applications in the development of new materials with specific characteristics. Its unique structure and properties can be leveraged to create materials with improved stability, reactivity, or other desirable traits for various applications.
Used in Chemical Stability Enhancement:
Due to its steric hindrance, Ethanone, 1-(2,2,3,3-tetramethylcyclopropyl)is used to enhance the stability of other chemical compounds, making them more resistant to degradation in different environments. This application is particularly relevant in industries where chemical stability is crucial for product performance and longevity.

Check Digit Verification of cas no

The CAS Registry Mumber 60802-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,0 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60802-86:
(7*6)+(6*0)+(5*8)+(4*0)+(3*2)+(2*8)+(1*6)=110
110 % 10 = 0
So 60802-86-0 is a valid CAS Registry Number.

60802-86-0Downstream Products

60802-86-0Relevant academic research and scientific papers

Experimental and Theoretical Investigations of Ring-Expansion in 1-Methylcyclopropylcarbene

Thamattoor, Dasan M.,Snoonian, John R.,Sulzbach, Horst M.,Hadad, Christopher M.

, p. 5886 - 5895 (2007/10/03)

1-Methylcyclopropylcarbene, generated by photolysis of two isomeric hydrocarbon precursors, undergoes ring-expansion, readily to give 1-methylcyclobutene. Experimentally, intramolecular carbon-hydrogen insertions are not observed. Trapping studies with TME demonstrates the formation of the expected cyclopropane adduct, and via a double-reciprocal analysis, the lifetime of 1-methylcyclopropylcarbene was determined to be 12 ns in 1,1,2-trichlorotrifluoroethane. Computational studies show that the barrier to ring-expansion is significantly smaller in 1-methylcyclopropylcarbene than in cyclopropylcarbene. The origin of the increased rate of ring-expansion is due to stabilization of the positive charge that occurs at the incipient tertiary carbon that is attached to the migrating carbon center. Department of Chemistry and Biochemistry,.

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