192863-46-0 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-Fluorophenyl)benzaldehyde is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-Fluorophenyl)benzaldehyde is utilized as an intermediate in the production of agrochemicals, potentially enhancing crop protection and yield.
Used in Dye Industry:
2-(4-FLUOROPHENYL)BENZALDEHYDE is employed as an intermediate in the synthesis of dyes, contributing to the creation of a wide range of colorants for various applications.
Used in Perfumery and Flavoring Industry:
2-(4-Fluorophenyl)benzaldehyde is used as a fragrance and flavoring agent due to its distinctive aromatic and aldehydic scent, adding depth and complexity to perfumes and flavorings.
Used in Chemical Reactions as a Building Block:
In the realm of chemical research and development, 2-(4-Fluorophenyl)benzaldehyde serves as a building block in the creation of new compounds for a variety of industrial applications, showcasing its versatility in chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 192863-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,8,6 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 192863-46:
(8*1)+(7*9)+(6*2)+(5*8)+(4*6)+(3*3)+(2*4)+(1*6)=170
170 % 10 = 0
So 192863-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H9FO/c14-12-7-5-10(6-8-12)13-4-2-1-3-11(13)9-15/h1-9H
192863-46-0Relevant articles and documents
Gold Catalysts Can Generate Nitrone Intermediates from a Nitrosoarene/Alkene Mixture, Enabling Two Distinct Catalytic Reactions: A Nitroso-Activated Cycloheptatriene/Benzylidene Rearrangement
Cheng, Mu-Jeng,Kardile, Rahul Dadabhau,Kuo, Tung-Chun,Liu, Rai-Shung,More, Sayaji Arjun
, p. 5506 - 5511 (2021/07/31)
Gold-catalyzed reactions of cycloheptatrienes with nitrosoarenes yield nitrone derivatives efficiently. This reaction sequence enables us to develop gold-catalyzed aerobic oxidations of cycloheptatrienes to afford benzaldehyde derivatives using CuCl and nitrosoarenes as co-catalysts (10-30 mol %). Our density functional theory calculations support a novel nitroso-activated rearrangement, tropylium → benzylidene. With the same nitrosoarenes, we developed their gold-catalyzed [2 + 2 + 1]-annulations between nitrosobenzene and two enol ethers to yield 5-alkoxyisoxazolidines using 1,4-cyclohexadienes as hydrogen donors.
