946402-23-9 Usage
Physical appearance
White to off-white solid The compound appears as a white to off-white solid substance.
Field of use
Organic chemistry and medicinal research It is utilized in the study and development of organic compounds and pharmaceuticals.
Chemical classification
Derivative of acetamide The compound is derived from acetamide, a basic structure in organic chemistry.
Structural components
Fluorophenyl, methoxy, and methyl groups The compound contains a fluorophenyl group (a phenyl ring with a fluorine atom), a methoxy group (an oxygen atom connected to a methyl group), and a methyl group attached to the nitrogen atom.
Potential applications
Pharmaceutical development The compound may be used in the creation of new pharmaceuticals due to its potential analgesic and anti-inflammatory properties.
Synthesizing building block
Synthesis of other organic compounds The compound can serve as a building block for the synthesis of other organic compounds, expanding its potential uses in various fields.
Research status
Further research needed More research is required to fully understand the potential uses and effects of 2-(2-fluorophenyl)-N-methoxy-N-methylacetamide.
Check Digit Verification of cas no
The CAS Registry Mumber 946402-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,4,0 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 946402-23:
(8*9)+(7*4)+(6*6)+(5*4)+(4*0)+(3*2)+(2*2)+(1*3)=169
169 % 10 = 9
So 946402-23-9 is a valid CAS Registry Number.
946402-23-9Relevant articles and documents
Iron-Catalyzed Enantioselective Radical Carboazidation and Diazidation of α,β-Unsaturated Carbonyl Compounds
Dong, Shunxi,Feng, Xiaoming,He, Jun,Liu, Wen,Liu, Xiaohua,Pu, Maoping,Wu, Yun-Dong,Zhang, Tinghui
supporting information, p. 11856 - 11863 (2021/08/16)
Azidation of alkenes is an efficient protocol to synthesize organic azides which are important structural motifs in organic synthesis. Enantioselective radical azidation, as a useful strategy to install a C-N3 bond, remains challenging due to the inherently instability and unique structure of radicals. Here, we disclose an efficient enantioselective radical carboazidation and diazidation of α,β-unsaturated ketones and amides catalyzed by chiral N,N′-dioxide/Fe(OTf)2 complexes. An array of substituted alkenes was transformed to the corresponding α-azido carbonyl derivatives in good to excellent enantioselectivities, benefiting the preparation of chiral α-amino ketones, vicinal amino alcohols, and vicinal diamines. Control experiments and mechanistic studies proved the radical pathway in the reaction process. The DFT calculations showed that the azido transferred to the radical intermediate via an intramolecular five-membered transition state with the internal nitrogen of the Fe-N3 species.
NOVEL AND IMPROVED PROCESSES FOR THE PREPARATION OF PRASUGREL, ITS INTERMEDIATES AND PHARMACEUTICALLY ACCEPTABLE SALTS
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Page/Page column 49, (2011/04/26)
The present invention relates to novel and improved processes for the preparation of prasugrel compound of formula-(1), its intermediates and pharmaceutically acceptable salts.
