69943-47-1 Usage
Description
(2-Chloro-4-fluorophenyl)phenylmethanone, also known as 4'-Chloro-4-fluorodiphenyl ketone, is a chemical compound with the molecular formula C13H8ClFO. It is a ketone derivative that consists of a phenyl group with a (2-chloro-4-fluorophenyl) substituent. (2-Chloro-4-fluorophenyl)phenylmethanone is used in various fields, including organic synthesis, pharmaceutical research, and materials science.
Uses
Used in Pharmaceutical Research:
(2-Chloro-4-fluorophenyl)phenylmethanone is used as a key intermediate in the synthesis of pharmaceutical drugs. Its unique structure allows for the development of new drug candidates with potential therapeutic applications.
Used in Agrochemicals:
In the agrochemical industry, (2-Chloro-4-fluorophenyl)phenylmethanone is used as a building block for the creation of new agrochemicals. Its properties contribute to the development of effective and targeted pest control solutions.
Used in Materials Science:
(2-Chloro-4-fluorophenyl)phenylmethanone is utilized in materials science for the development of novel materials with specific properties. Its incorporation into these materials can lead to advancements in various applications, such as coatings, adhesives, and polymers.
Used as an Intermediate in Organic Synthesis:
(2-Chloro-4-fluorophenyl)phenylmethanone serves as an intermediate in the production of various organic compounds. Its versatility in chemical reactions makes it a valuable component in the synthesis of a wide range of molecules.
It is important to handle (2-Chloro-4-fluorophenyl)phenylmethanone with caution, as it may have hazardous effects on human health and the environment. Proper safety measures should be taken during its use and disposal to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 69943-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,4 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69943-47:
(7*6)+(6*9)+(5*9)+(4*4)+(3*3)+(2*4)+(1*7)=181
181 % 10 = 1
So 69943-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H8ClFO/c14-12-8-10(15)6-7-11(12)13(16)9-4-2-1-3-5-9/h1-8H
69943-47-1Relevant articles and documents
Transition-metal-free carbonylation of aryl halides with arylboronic acids by utilizing stoichiometric CHCl3 as the carbon monoxide-precursor
Xu, Fangning,Li, Dan,Han, Wei
supporting information, p. 2911 - 2915 (2019/06/18)
Under transition-metal-free conditions, carbonylative Suzuki couplings of aryl halides with arylboronic acid using stoichiometric CHCl3 as the carbonyl source has been developed. The simple, efficient, and environmentally benign method was successfully applied to the synthesis of Fenofibric acid, naphthyl phenstatin, and carbon-13 labeled biaryl ketone.
Synthesis of structurally diverse diarylketones through the diarylmethyl sp3 C-H oxidation
He, Chao,Zhang, Xiaohui,Huang, Ruofeng,Pan, Jing,Li, Jiaqiang,Ling, Xuege,Xiong, Yan,Zhu, Xiangming
, p. 4458 - 4462 (2014/08/05)
Under open-flask conditions, an efficient method to assemble a series of diversely functionalized diarylketones in the presence of commercially available NBS has been developed. Yields of up to 99% have been achieved employing diarylmethanes as starting material. Based on 18O-labeled experiment, the addition of stoichiometric water eventually leads to excellent yields in all carbonylation cases.
The synthesis and electronic absorption spectra of 3-phenyl-3(4- pyrrolidino-2-substituted phenyl)-3H-naphtho[2,1-b]pyrans: Further exploration of the ortho substituent effect
Gabbutt, Christopher D.,Heron, B. Mark,Instone, Alicia C.
, p. 737 - 745 (2007/10/03)
Introduction of a substituent into a sterically demanding 2-position of a 3-(4-pyrrolidinophenyl) ring of a 3,3-diaryl-3H-naphtho[2,1-b]pyran results in the generation of an additional short wavelength absorption band leading to organic photochromes that