3184-61-0 Usage
Uses
Used in Organic Synthesis:
4-(1,3-dioxoisoindol-2-yl)butanenitrile is utilized as a key intermediate in organic synthesis for the creation of a variety of organic compounds. Its structural features facilitate its use in the formation of complex organic molecules, making it a versatile component in chemical reactions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(1,3-dioxoisoindol-2-yl)butanenitrile serves as a building block for the synthesis of pharmaceuticals. Its chemical properties allow it to be incorporated into the structures of potential new drugs, contributing to the discovery and development of novel therapeutic agents.
Used in Drug Development:
4-(1,3-dioxoisoindol-2-yl)butanenitrile is employed in the development of new drugs due to its compatibility with various chemical reactions and its potential to enhance the pharmacological properties of drug candidates. Its presence in a compound can influence aspects such as solubility, stability, and bioavailability, which are critical for drug efficacy and safety.
Used in Bioactive Compounds Research:
4-(1,3-dioxoisoindol-2-yl)butanenitrile is also used in the research of bioactive compounds, where its unique structure can contribute to the discovery of substances with specific biological activities. Its ability to be modified and incorporated into diverse molecular frameworks makes it a promising candidate for the exploration of new bioactive substances with potential applications in medicine and healthcare.
Check Digit Verification of cas no
The CAS Registry Mumber 3184-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3184-61:
(6*3)+(5*1)+(4*8)+(3*4)+(2*6)+(1*1)=80
80 % 10 = 0
So 3184-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2O2/c13-7-3-4-8-14-11(15)9-5-1-2-6-10(9)12(14)16/h1-2,5-6H,3-4,8H2
3184-61-0Relevant academic research and scientific papers
Preparation method of alkyl nitrile compound
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Paragraph 0214-0216, (2020/08/18)
The invention discloses a preparation method of an alkyl nitrile compound. Specifically, the preparation method comprises the following step: in an organic solvent, in the presence of a protective gasand under the action of a catalyst, carrying out a reduction reaction as shown in the specification on olefin as shown in a formula I, a cyanation reagent and water, wherein the alkyl nitrile compound 1 is a compound II and/or a compound III. The preparation method provided by the invention is mild in condition, can realize hydrocyanation of olefin more safely and efficiently, and has good substrate universality and functional group compatibility.
Cleavage of carbon-carbon triple bond: Direct transformation of alkynes to nitriles
Okamoto, Noriko,Ishikura, Minoru,Yanada, Reiko
, p. 2571 - 2573 (2013/07/11)
A new cleavage reaction of carbon-carbon triple bonds proceeds efficiently with NIS and TMSN3, giving the corresponding nitriles in moderate to good yields.
