5342-96-1 Usage
Uses
Used in Pharmaceutical Industry:
4-Benzoyl-4-(2-cyanoethyl)heptanedinitrile is utilized as a starting material for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it suitable for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Benzoyl-4-(2-cyanoethyl)heptanedinitrile is employed as a precursor in the production of agrochemical compounds. Its role in the synthesis of these compounds contributes to the development of effective agricultural chemicals for pest control and crop protection.
Used in Dye and Pigment Production:
4-Benzoyl-4-(2-cyanoethyl)heptanedinitrile is also used in the manufacturing process of dyes and pigments. Its chemical properties allow for the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing.
Used in Other Industrial Applications:
Beyond its primary uses in pharmaceuticals, agrochemicals, and dyes, 4-Benzoyl-4-(2-cyanoethyl)heptanedinitrile finds application in several other industrial sectors. Its versatility and chemical characteristics make it a valuable component in the production of various chemical products, contributing to the advancement of multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5342-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5342-96:
(6*5)+(5*3)+(4*4)+(3*2)+(2*9)+(1*6)=91
91 % 10 = 1
So 5342-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H17N3O/c18-12-4-9-17(10-5-13-19,11-6-14-20)16(21)15-7-2-1-3-8-15/h1-3,7-8H,4-6,9-11H2
5342-96-1Relevant academic research and scientific papers
Bolte, Michael,Scholtyssik, Maria
, p. 852 - 854 (1998)
The title compound, C17H17N3O, crystallizes with two molecules in the asymmetric unit which differ significantly only in the conformation of one torsion angle. All bonds between the methylenic C atoms display antiperiplana
Enviornmentally benign michael and claisen schmidt reaction of aromatic carbonyl compounds by alkaline polyionic resin
Jaitak, Vikas,Kaul,Das, Pralay
, p. 1137 - 1145 (2013/09/24)
A regioselective Michael reaction between aryl methyl ketones and α,β-unsaturated compounds has been carried out using basic polyionic resin as a reusable reagent. Results indicate that the reaction proceeds in consecutive manner as double Michael (27-65%) and triple Michael (40-45%) products with overall yields of 55-80%. Moreover, A-2XMP resin has also been applied on Claisen Schmidt condensations of aromatic aldehydes and ketones (acyclic as well as cyclic) under different reaction conditions yielding dehydrated products in 82-94% yield. The reactions give an opportunity for easy separation, reusability of polyionic resin and easy purification of products in continuous or multiple processing of organic compounds.
One-pot multicomponent Michael and Thorpe-Ziegler reaction of aryl methyl ketones
Jaitak, Vikas,Bandna,Das, Pralay,Kaul,Singh, Bikram,Kumar, Neeraj
experimental part, p. 2727 - 2737 (2011/09/15)
A regioselective base-promoted Michael and Thorpe-Ziegler reaction between aryl methyl ketones and αβ-unsaturated nitrile was carried out in a single step. Different functional groups in addition to active positions were tolerated under this condition. Re
