7136-23-4 Usage
Uses
Used in Organic Synthesis:
2,3,3-Triphenyloxirane-2-carbonitrile is used as a building block in the preparation of various pharmaceuticals and other organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry Research:
Due to its biological activity, 2,3,3-triphenyloxirane-2-carbonitrile is of interest in medicinal chemistry research. It can be further modified or used as a starting material to develop new drugs with potential therapeutic applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3,3-triphenyloxirane-2-carbonitrile is used as an intermediate in the synthesis of various drugs. Its versatility in organic synthesis allows for the development of new pharmaceutical compounds with improved efficacy and safety profiles.
It is important to handle 2,3,3-triphenyloxirane-2-carbonitrile with care, as it may pose health hazards if not used properly. Proper safety measures should be taken during its synthesis, storage, and use to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 7136-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7136-23:
(6*7)+(5*1)+(4*3)+(3*6)+(2*2)+(1*3)=84
84 % 10 = 4
So 7136-23-4 is a valid CAS Registry Number.
7136-23-4Relevant academic research and scientific papers
Double duty for cyanogen bromide in a cascade synthesis of cyanoepoxides
Li, Zhou,Gevorgyan, Vladimir
supporting information; experimental part, p. 2808 - 2810 (2011/05/05)
An unprecedented reaction mode of cyanogen bromide has been discovered. Under basic conditions, cyanogen bromide acts as an equivalent of both Br + and CN- to convert enolizable ketones into the corresponding cyanoepoxides in good yields. This unique reaction mode provides new, one-pot access to densely substituted cyanoepoxides from easily available ketones (see scheme). Copyright
