70783-44-7 Usage
Uses
Used in Pharmaceutical Industry:
2,2,2-Trifluoro-1-[4-(morpholin-4-yl)phenyl]ethan-1-one is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of biologically active compounds. Its unique structure allows for the creation of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2,2-trifluoro-1-[4-(morpholin-4-yl)phenyl]ethan-1-one is utilized as an intermediate in the production of agrochemicals, enabling the synthesis of compounds with pesticidal or herbicidal properties, thereby contributing to crop protection and yield enhancement.
Used in Medicinal Chemistry Research:
2,2,2-Trifluoro-1-[4-(morpholin-4-yl)phenyl]ethan-1-one serves as a valuable tool in medicinal chemistry research, where its unique properties are harnessed to explore new avenues in drug discovery and the design of novel therapeutic agents.
Used in Synthetic Chemistry Research:
2,2,2-trifluoro-1-[4-(morpholin-4-yl)phenyl]ethan-1-one is also used in synthetic chemistry research, where its structural attributes facilitate the synthesis of complex organic molecules and the investigation of reaction mechanisms, further expanding the scope of chemical knowledge and application.
Check Digit Verification of cas no
The CAS Registry Mumber 70783-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,8 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70783-44:
(7*7)+(6*0)+(5*7)+(4*8)+(3*3)+(2*4)+(1*4)=137
137 % 10 = 7
So 70783-44-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H12F3NO2/c13-12(14,15)11(17)9-1-3-10(4-2-9)16-5-7-18-8-6-16/h1-4H,5-8H2
70783-44-7Relevant academic research and scientific papers
A practical method for the preparation of 4-nitrogen-substituted benzoic acids
Shinozuka, Tsuyoshi,Nakao, Akira,Saito, Keiji,Naito, Satoru
, p. 1090 - 1091 (2007/10/03)
An efficient and practical method for the preparation of 4-nitrogen-substituted benzoic acids is described. Our method consists of the aromatic substitution of 2,2,2,4′-tetrafluoroacetophenone with amines, followed by haloform reaction to the benzoic acids. In this method, even though for the less nucleophilic 7-, 8-, and 9-membered amines 1 equiv. was used, corresponding benzoic acids were obtained in moderate to excellent yield. As the experimental procedure including purification is simple, this method is applicable to large-scale syntheses. Copyright
