54648-47-4 Usage
General Description
The chemical compound (2Z)-2-(4-fluorophenyl)-3-phenylacrylonitrile is a nitrile derivative with a molecular formula C17H10FN. It is a yellow, crystalline solid with a molecular weight of 250.26 g/mol. (2Z)-2-(4-FLUOROPHENYL)-3-PHENYLACRYLONITRILE is used in organic synthesis and as a building block for the preparation of various pharmaceuticals and agrochemicals. It is also known to exhibit potent biological activities, making it a valuable intermediate in the production of therapeutic agents. Additionally, (2Z)-2-(4-fluorophenyl)-3-phenylacrylonitrile is used in the field of material science for the production of polymers and advanced materials. However, it is important to handle this compound with caution, as it may pose health risks if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 54648-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,4 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54648-47:
(7*5)+(6*4)+(5*6)+(4*4)+(3*8)+(2*4)+(1*7)=144
144 % 10 = 4
So 54648-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H10FN/c16-15-8-6-13(7-9-15)14(11-17)10-12-4-2-1-3-5-12/h1-10H/b14-10+
54648-47-4Relevant articles and documents
Pd(II)-Catalyzed CC Bond Cleavage by a Formal Group-Exchange Reaction
Ye, Runyou,Zhu, Maoshuai,Yan, Xufei,Long, Yang,Xia, Ying,Zhou, Xiangge
, p. 8678 - 8683 (2021/07/26)
A chelation-assisted palladium-catalyzed CC bond cleavage of α, β-unsaturated ketone to form alkenyl nitrile in the presence of nitrile is disclosed on the basis of a formal group-exchange reaction formulated as C1C2 + C3 → C1C3 + C2, differing from normal alkene oxidative cleavage and metathesis type. The isolated key active Pd(II) complex as well as deuterium-labeled experiment revealed the necessity of the chelation group, and a plausible catalytic pathway was proposed.
Kinetic Study of the Base-catalysed Reactions of Benzaldahehyde and Thiophene-2-carbaldehyde with Acetonitriles
Alberghina, Gaetano,Amato, Maria Emanuela,Corsaro, Antonio,Fisichella, Salvatore,Scarlata, Giuseppe
, p. 353 - 356 (2007/10/02)
The reaction rates of the sodium methoxide-catalysed condensation of benzaldehyde and thiophene-2-carbaldehyde with heteroaromatic acetonitriles ArCH2CN; Ar = C6H5, C6H4CH3(p), C6H4-OCH3(p), C6H4F(p), C6H4Cl(p), C6H4Br(p), 2-thienyl, 3-thienyl, 3-pyridyl
