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4-chloro-1-phenylpentan-1-one is an organic compound with the molecular formula C11H13ClO. It is a colorless to pale yellow liquid with a distinct aromatic odor. This chemical is characterized by the presence of a chloro group (-Cl) at the 4th carbon position, a phenyl group (C6H5) attached to the 1st carbon, and a ketone functional group (C=O) at the 1st carbon as well. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential applications, 4-chloro-1-phenylpentan-1-one is an important compound in the field of organic chemistry.

4831-02-1

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4831-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4831-02-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4831-02:
(6*4)+(5*8)+(4*3)+(3*1)+(2*0)+(1*2)=81
81 % 10 = 1
So 4831-02-1 is a valid CAS Registry Number.

4831-02-1Relevant academic research and scientific papers

Silver-catalyzed decarboxylative chlorination of aliphatic carboxylic acids

Wang, Zhentao,Zhu, Lin,Yin, Feng,Su, Zhongquan,Li, Zhaodong,Li, Chaozhong

experimental part, p. 4258 - 4263 (2012/04/10)

Decarboxylative halogenation of carboxylic acids, the Hunsdiecker reaction, is one of the fundamental functional group transformations in organic chemistry. As the initial method requires the preparations of strictly anhydrous silver carboxylates, several modifications have been developed to simplify the procedures. However, these methods suffer from the use of highly toxic reagents, harsh reaction conditions, or limited scope of application. In addition, none is catalytic for aliphatic carboxylic acids. In this Article, we report the first catalytic Hunsdiecker reaction of aliphatic carboxylic acids. Thus, with the catalysis of Ag(Phen)2OTf, the reactions of carboxylic acids with t-butyl hypochlorite afforded the corresponding chlorodecarboxylation products in high yields under mild conditions. This method is not only efficient and general, but also chemoselective. Moreover, it exhibits remarkable functional group compatibility, making it of more practical value in organic synthesis. The mechanism of single electron transfer followed by chlorine atom transfer is proposed for the catalytic chlorodecarboxylation.

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