50690-09-0 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) is also utilized in the production of agrochemicals, specifically as a precursor in the synthesis of pesticides and other agricultural chemicals. Its reactivity and structural features make it suitable for the creation of effective and targeted agrochemical products.
Used in Dyes and Fragrances Industry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) is employed in the formulation of dyes and fragrances due to its aromatic properties. Its ability to impart color and scent to various products makes it a valuable component in this industry.
Used as a Reagent in Organic Chemistry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) may also have potential applications as a reagent in organic chemistry reactions. Its reactivity and functional groups can be harnessed to facilitate various chemical transformations and synthesis processes.
It is important to handle Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) with caution, as it may have potential health hazards and should be used with proper safety measures.
Check Digit Verification of cas no
The CAS Registry Mumber 50690-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,9 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50690-09:
(7*5)+(6*0)+(5*6)+(4*9)+(3*0)+(2*0)+(1*9)=110
110 % 10 = 0
So 50690-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO/c1-2-8-3-5-9(6-4-8)10(12)7-11/h3-6H,2,7H2,1H3
50690-09-0Relevant academic research and scientific papers
AuIII-Catalyzed Formation of α-Halomethyl Ketones from Terminal Alkynes
Xing, Yalan,Zhang, Ming,Ciccarelli, Sarah,Lee, John,Catano, Bryant
supporting information, p. 781 - 785 (2017/02/15)
A AuIII-catalyzed synthesis of α-halomethyl ketones from terminal alkynes was developed. This approach features excellent functional group compatibility and good yields for both aromatic and aliphatic terminal alkynes. The resulting α-halomethyl ketones were used to prepare heterocyclic indolizine structures. The plausible mechanism of the one-pot reaction is proposed.
Metal-free hydration of aromatic haloalkynes to α-halomethyl ketones
Ye, Min,Wen, Yuelu,Li, Huifang,Fu, Yejuan,Wang, Qinghao
supporting information, p. 4983 - 4986 (2016/10/21)
A highly regioselective and efficient metal-free hydration of aromatic haloalkynes to α-halomethyl ketones using cheap tetrafluoroboric acid as catalyst is described. The protocol is conducted under convenient conditions and affords products in good to excellent yields, with broad substrate scope, including a variety of aromatic alkynyl chlorides, alkynyl bromides, and alkynyl iodides.
α-Chlorination of Aromatic Acetyl Derivatives with Benzyltrimethylammonium Dichloroiodate
Kajigaeshi, Shoji,Kakinami, Takaaki,Moriwaki, Masayuki,Fujisaki, Shizuo,Maeno, Kimihiro,Okamoto, Tsuyoshi
, p. 545 - 546 (2007/10/02)
Reaction of aromatic acetyl derivatives with benzyltrimethylammonium dichloroiodate in refluxing dichloroethane/methanol for several hours gave α-chloroacetyl derivatives in good yields.
