23293-77-8 Usage
Uses
Used in Pharmaceutical Industry:
Cyclohexanol, 1-ethynyl-, 1-benzoate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the creation of complex organic molecules. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, Cyclohexanol, 1-ethynyl-, 1-benzoate is utilized as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its versatility in organic synthesis enables the development of effective and targeted agrochemicals for agricultural applications.
Used in Organic Chemistry Research:
Cyclohexanol, 1-ethynyl-, 1-benzoate is used as a valuable building block in organic chemistry research for its ability to form a wide range of organic compounds. It is employed in the development of new synthetic methods and the exploration of novel chemical reactions.
Used in Specialty Chemicals Production:
Cyclohexanol, 1-ethynyl-, 1-benzoate is used in the production of specialty chemicals, such as fragrances, dyes, and other high-value organic compounds. Its unique properties and reactivity make it an essential component in the synthesis of these specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 23293-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,9 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23293-77:
(7*2)+(6*3)+(5*2)+(4*9)+(3*3)+(2*7)+(1*7)=108
108 % 10 = 8
So 23293-77-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O2/c1-2-15(11-7-4-8-12-15)17-14(16)13-9-5-3-6-10-13/h1,3,5-6,9-10H,4,7-8,11-12H2
23293-77-8Relevant academic research and scientific papers
Neighboring Carbonyl Group Assisted Oxyacetoxylation of Propargylic Carboxylates with Retention of Chirality under Metal Free Condition
Pradhan, Tapas R.,Mohapatra, Debendra K.
supporting information, p. 3605 - 3611 (2019/07/04)
A metal-free oxyacetoxylation method of primary, secondary and tertiary propargylic carboxylates with retention of chirality was presented. The reaction proceeds through the intramolecular nucleophilic attack of the neighboring carbonyl group on an alkynyliodonium intermediate. The process is general with broad substrate scope and is amenable for application to a variety of propargyl carboxylates including those obtained from natural products. Insight into the mechanistic pathway by isotopic labelling (using H2O18 and D2O) and controlled experiments confirmed. (Figure presented.).
