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3-((4-chlorophenyl)amino)-3-(4-fluorophenyl)-1-phenylpropan-1-one is a complex organic compound with the molecular formula C25H20ClFNO. It is a derivative of propanone, featuring a 4-chlorophenyl and 4-fluorophenyl group attached to the nitrogen atom of an amino group, and a phenyl group attached to the carbonyl carbon. 3-((4-chlorophenyl)amino)-3-(4-fluorophenyl)-1-phenylpropan-1-one is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its structure and properties make it a versatile building block for the development of new chemical entities with potential therapeutic benefits.

2046-99-3

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2046-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2046-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2046-99:
(6*2)+(5*0)+(4*4)+(3*6)+(2*9)+(1*9)=73
73 % 10 = 3
So 2046-99-3 is a valid CAS Registry Number.

2046-99-3Downstream Products

2046-99-3Relevant academic research and scientific papers

Choline-based biodegradable ionic liquid catalyst for Mannich-type reaction

Huan, Peng,Yulin, Hu,Rong, Xing,Dong, Fang

, p. 1855 - 1860 (2016)

A three-component Mannich-type reaction of aromatic aldehydes, ketones, and amines was catalyzed by a novel choline-based acidic ionic liquid. The proposed catalyst was a Lewis-Br?nsted dual acid catalyst as well as water-tolerant. The β-amino carbonyl compounds were obtained at room temperature in reasonable to good yields ranging from 63 to 98%. After the reaction, the catalyst could be recycled and reused for 5 times without obvious decrease of the yield. Further, the catalyst was environment-friendly with a significant biodegradation rate. [Figure not available: see fulltext.]

Br?nsted-Lewis dual acidic ionic liquid immobilized on mesoporous silica materials as an efficient cooperative catalyst for Mannich reactions

Wang, Hong Bo,Yao, Nan,Wang, Long,Hu, Yu Lin

supporting information, p. 10528 - 10531 (2017/10/03)

Novel mesoporous silica supported ILs have been prepared and successfully applied as a heterogeneous catalyst in Mannich reactions. The excellent recyclability of the supported catalyst, mild reaction conditions, good to excellent yields, low catalyst loading, and operational simplicity are the important features of this methodology.

Reusable 1,2,4-triazolium based bronsted acidic room temperature ionic liquids as catalyst for mannich base reaction

Nagarajan, Sankaranarayanan,Kandasamy, Elango

, p. 1507 - 1514,8 (2014/10/15)

Unprecedented examples of 1-alkyl-1,2,4-triazolium methanesulfonate based Bronsted acidic room temperature ionic liquids were synthesized and characterized. Their catalytic activity and efficiency in recyclability and reusability on one pot synthesis of halide substituted β-amino carbonyl compounds are reported. Graphical Abstract: [Figure not available: see fulltext.]

Highly efficient one-pot synthesis, antimicrobial and docking studies of newer β-amino carbonyl derivatives catalyzed by silica sulfuric acid

El-Bayouki,Basyouni,El-Sayed,Tohamy,El-Henawy

, p. 255 - 268 (2013/01/15)

Mannich reaction was applied between 4-fluorobezaldehyde, selected acetophenone and several anilines, catalyzed by silica sulfuric acid for the synthesis of β-amino carbonyl derivatives. Reaction time and yield of the products depended on the nature of ac

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