7391-58-4 Usage
Description
Butylmalononitrile, with the molecular formula C9H15N, is a colorless to pale yellow liquid characterized by a fruity odor. It serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, and as a building block in the preparation of heterocyclic compounds. Its reactivity and versatility are highlighted by its use in various chemical reactions, including Knoevenagel condensation, Michael addition, and nucleophilic addition. Butylmalononitrile also shows promise in the development of photoluminescent materials and as a precursor for dyes and pigments. Its potential antimicrobial and anti-inflammatory properties have garnered interest in medicinal chemistry.
Uses
Used in Pharmaceutical and Agrochemical Production:
Butylmalononitrile is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, leveraging its reactivity and versatility to facilitate the production of these compounds.
Used in Organic Synthesis:
As a building block in organic synthesis, Butylmalononitrile is used in the preparation of heterocyclic compounds, contributing to the development of novel chemical entities.
Used in Chemical Reactions:
Butylmalononitrile is employed in a wide range of chemical reactions such as Knoevenagel condensation, Michael addition, and nucleophilic addition, demonstrating its utility in diverse synthetic pathways.
Used in the Development of Photoluminescent Materials:
Butylmalononitrile is utilized in the research and development of photoluminescent materials, indicating its potential applications in optoelectronic and sensor technologies.
Used as a Precursor for Dyes and Pigments:
Butylmalononitrile serves as a precursor in the synthesis of various dyes and pigments, contributing to the coloration and decoration of a variety of products.
Used in Medicinal Chemistry for Antimicrobial and Anti-inflammatory Properties:
Due to its potential antimicrobial and anti-inflammatory properties, Butylmalononitrile is a subject of interest in medicinal chemistry, with potential applications in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 7391-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7391-58:
(6*7)+(5*3)+(4*9)+(3*1)+(2*5)+(1*8)=114
114 % 10 = 4
So 7391-58-4 is a valid CAS Registry Number.
7391-58-4Relevant articles and documents
Radical trifunctionalization of hexenenitrile via remote cyano migration
Chang, Chenyang,Wu, Xinxin,Zhang, Huihui,Zhu, Chen
supporting information, p. 1005 - 1008 (2022/02/01)
A novel radical-mediated trifunctionalization of hexenenitriles via the strategy of remote functional group migration is disclosed. A portfolio of functionalized hexenenitriles are employed as substrates. After difunctionalization of the unactivated alken
Sodium borohydride as the only reagent for the efficient reductive alkylation of malononitrile with ketones and aldehydes
Dunham, Jason C.,Richardson, Adam D.,Sammelson, Robert E.
, p. 680 - 686 (2007/10/03)
An efficient and convenient method for the synthesis of primary and secondary monosubstituted malononitriles has been developed. In this method, sodium borohydride in isopropanol has a catalytic effect on the initial condensation between malononitrile and
A facile method for the construction of highly substituted acetonitriles and olefins. Malononitriles as acetonitrile carbanion and alkylidene dianion equivalents
Tsai, Ting-Yueh,Shia, Kak-Shan,Liu, Hsing-Jang
, p. 97 - 101 (2007/10/03)
The use of malononitrile to facilitate the preparation of highly substituted nitriles, via reductive alkylation/addition, and olefins, via a combination of reductive addition and reductive elimination, is described.
