42413-59-2 Usage
Description
1-(4-Chlorophenyl)-1-phenylacetone, also known as 4'-Chloroacetophenone, is a chemical compound with the formula C16H13ClO. It is a white solid that exhibits a strong, sweet odor. 1-(4-Chlorophenyl)-1-phenylacetone is primarily recognized for its role in the synthesis of pharmaceuticals and other organic compounds, and it is also known for its use in the illicit production of amphetamines and other stimulant drugs.
Uses
Used in Pharmaceutical Industry:
1-(4-Chlorophenyl)-1-phenylacetone is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the creation of complex organic molecules that are otherwise difficult to produce.
Used in Perfumery:
In the fragrance industry, 1-(4-Chlorophenyl)-1-phenylacetone is used as a fixative or scent component due to its distinct, sweet odor, which helps to enhance and prolong the scent of perfumes and other fragranced products.
Used in Organic Chemistry:
1-(4-Chlorophenyl)-1-phenylacetone serves as a reagent in various organic chemical reactions, where it can act as a precursor to other compounds or participate in reactions that lead to the formation of desired products.
Used in Illicit Drug Production:
Regrettably, 1-(4-Chlorophenyl)-1-phenylacetone is also known for its use in the illicit production of amphetamines and other stimulant drugs, highlighting the dual nature of its applications and the need for regulatory oversight in its distribution and use.
Check Digit Verification of cas no
The CAS Registry Mumber 42413-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42413-59:
(7*4)+(6*2)+(5*4)+(4*1)+(3*3)+(2*5)+(1*9)=92
92 % 10 = 2
So 42413-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H13ClO/c1-11(17)15(12-5-3-2-4-6-12)13-7-9-14(16)10-8-13/h2-10,15H,1H3
42413-59-2Relevant articles and documents
Anodic oxidation triggered divergent 1,2- And 1,4-group transfer reactions of β-hydroxycarboxylic acids enabled by electrochemical regulation
Jiang, Yangye,Lu, Gang,Mo, Fanyang,Yang, Jianxin,Yang, Yang,Yin, Yunxing,Zeng, Chengchu,Zhang, Lei,Zhang, Xianhao,Zhang, Zhenxing
, p. 12021 - 12028 (2020/11/26)
We report a set of electrochemically regulated protocols for the divergent synthesis of ketones and β-keto esters from the same β-hydroxycarboxylic acid starting materials. Enabled by electrochemical control, the anodic oxidation of carboxylic acids proceeded in either a one-electron or a two-electron pathway, leading to a 1,4-aryl transfer or a semipinacol-type 1,2-group transfer product with excellent chemoselectivity. The 1,4-aryl transfer represents an unprecedented example of carbon-to-oxygen group transfer proceeding via a radical mechanism. In contrast to previously reported radical group transfer reactions, this 1,4-group transfer process features the migration of electron-rich aryl substituents. Furthermore, with these chemoselective electrochemical oxidation protocols, a range of ketones and β-keto esters including those possessing a challenging-to-access medium-sized ring could be synthesized in excellent yields. This journal is