4913-75-1 Usage
Uses
Used in Pharmaceutical Industry:
(4-amino-3-chlorophenyl)(phenyl)methanone is used as a chemical intermediate for the synthesis of various pharmaceutical drugs and chemicals. It plays a crucial role in the development of new medications and contributes to the advancement of the pharmaceutical field.
Used in Chemical Industry:
In the chemical industry, (4-amino-3-chlorophenyl)(phenyl)methanone is utilized as an intermediate in the production of organic compounds. Its unique structure allows for the creation of a wide range of chemical products, making it a valuable asset in the chemical synthesis process.
Safety Precautions:
It is important to handle (4-amino-3-chlorophenyl)(phenyl)methanone with care, as it may cause irritation to the respiratory system, skin, or eyes upon contact. Additionally, it is crucial to consult with a professional before handling or using this chemical in any experimental or industrial setting to ensure proper safety measures are taken.
Check Digit Verification of cas no
The CAS Registry Mumber 4913-75-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4913-75:
(6*4)+(5*9)+(4*1)+(3*3)+(2*7)+(1*5)=101
101 % 10 = 1
So 4913-75-1 is a valid CAS Registry Number.
4913-75-1Relevant academic research and scientific papers
Coumarin-surfactant modified polyoxometalate catalyzed cross dehydrogenative coupling of benzyl alcohol with the: Para -C-H of unprotected aniline
Xu, Qian,Yu, Gang,Liu, Min,Peng, Chang,Banks, M. Katherine,Xu, Weijian,Wu, Ruoxi,Lu, Yanbing
, p. 5133 - 5136 (2018/10/24)
This paper presents a novel method for synthesizing para-aminobenzophenone and its derivatives (p-ABPs) using a coumarin-surfactant modified polyoxometalate as the catalyst. Preliminary mechanistic studies indicate that the reaction has undergone an oxidative cross dehydrogenative coupling process. This method has the advantages of an easy process, a convenient raw material source, safe and green oxidants, and tolerances of several functional groups.
