7496-27-7 Usage
Uses
Used in Organic Synthesis:
(2Z)-2-(4-methylphenyl)-3-phenylprop-2-enenitrile is utilized as a key intermediate in organic synthesis for the development of new compounds with diverse applications. Its unique structure allows for various chemical reactions, facilitating the creation of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2Z)-2-(4-methylphenyl)-3-phenylprop-2-enenitrile serves as a valuable compound for drug discovery and development. Its potential biological activities and reactivity make it a promising candidate for the synthesis of new pharmaceutical agents, targeting a range of therapeutic areas.
Used in Industry and Material Science:
(2Z)-2-(4-methylphenyl)-3-phenylprop-2-enenitrile may also find applications in industry and material science due to its chemical properties. Its use could be directed towards the development of new materials with specific characteristics, such as improved stability or reactivity, depending on the requirements of various industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 7496-27-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7496-27:
(6*7)+(5*4)+(4*9)+(3*6)+(2*2)+(1*7)=127
127 % 10 = 7
So 7496-27-7 is a valid CAS Registry Number.
7496-27-7Relevant academic research and scientific papers
Synthesis of non-symmetrical 3,4-diaryl-substituted pyrroles: Implementation for the preparation of lamellarin R
Zavala-Gómez, Héctor,Ramírez-Rodríguez, Armando,Vázquez, Alfredo
, p. 677 - 683 (2018/01/08)
A straightforward method for synthesising symmetrical and non-symmetrical 3,4-diaryl-substituted pyrroles is proposed, consisting of (i) the condensation reaction between phenylacetonitriles and aldehydes to give acrylonitriles, (ii) the conjugate additio
A Paal-Knorr approach to 3,4-diaryl-substituted pyrroles: Facile synthesis of lamellarins O and Q
Ramirez-Rodriguez, Armando,Mendez, Jose M.,Jimenez, Cristina C.,Leon, Fernando,Vazquez, Alfredo
, p. 3321 - 3326,6 (2012/12/12)
A very simple, yet efficient synthetic methodology, to obtain 3,4-diaryl-substituted pyrroles is described. The approach is based on the Knoevenagel condensation between arylacetonitriles and substituted aromatic aldehydes, followed by conjugate addition of cyanide to afford succinonitriles in excellent yields. The products thus obtained were subjected to DIBAL-H reduction, followed by cyclization under acidic conditions to produce the corresponding pyrroles in good overall yields. The utility of this protocol is exemplified by the synthesis of the marine alkaloids lamellarins O and Q.
