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[1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethylis a chemical compound characterized by its molecular formula C20H26O2. It features a cyclic ketone structure with a bicyclohexyl framework and a dimethyl substitution at the 1,1' positions. [1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethylis utilized in various fields, including organic synthesis and as a reagent in chemical reactions. It also holds potential for applications in the pharmaceutical, agrochemical, and materials science industries. However, it is crucial to handle [1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethyl- with caution due to its potential health and environmental risks if mismanaged.

1923-16-6

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1923-16-6 Usage

Uses

Used in Organic Synthesis:
[1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethylis used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure and reactivity make it a valuable building block for creating complex molecules.
Used in Chemical Reactions:
As a reagent, [1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethylis employed in a range of chemical reactions to facilitate specific transformations. Its role in these processes is to act as a catalyst or to participate in the formation of new chemical bonds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, [1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethylis used as a starting material or a component in the development of new drugs. Its structural properties allow for the creation of novel therapeutic agents with potential applications in treating various medical conditions.
Used in Agrochemical Industry:
[1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethylis also utilized in the agrochemical industry, where it serves as a precursor for the synthesis of various agrochemical products, such as pesticides and herbicides. Its contribution to the development of these products helps improve agricultural practices and crop protection.
Used in Materials Science:
Within the field of materials science, [1,1'-Bicyclohexyl]-2,2'-dione, 1,1'-dimethylis used to develop new materials with specific properties. Its incorporation into the synthesis of polymers, composites, and other materials can lead to the creation of innovative products with enhanced performance characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 1923-16-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1923-16:
(6*1)+(5*9)+(4*2)+(3*3)+(2*1)+(1*6)=76
76 % 10 = 6
So 1923-16-6 is a valid CAS Registry Number.

1923-16-6Downstream Products

1923-16-6Relevant academic research and scientific papers

Oxovanadium-Induced Oxidative Desilylation for the Selective Synthesis of 1,4-Diketones

Fujii Takashi,Hirao, Toshikazu,Ohshiro, Yoshiki

, p. 5823 - 5826 (2007/10/02)

Silyl enol ethers underwent the VO(OR)Cl2-induced homo- or cross-coupling giving 1,4-diketones selectively via one-electron oxidative desilylation.

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