5428-58-0 Usage
Uses
Used in Pharmaceutical Industry:
2-(dimethylamino)-1,4-diphenylbutane-1,4-dione is used as a building block for the synthesis of pharmaceuticals due to its versatile chemical structure, which can be incorporated into various drug molecules to enhance their therapeutic effects.
Used in Organic Synthesis:
In the field of organic chemistry, 2-(dimethylamino)-1,4-diphenylbutane-1,4-dione is utilized as a key intermediate in the synthesis of complex organic compounds, contributing to the development of new materials and chemical entities.
Used in Research and Development:
2-(dimethylamino)-1,4-diphenylbutane-1,4-dione is also employed in research settings to study its anti-inflammatory and analgesic properties, potentially leading to the discovery of new therapeutic agents for pain and inflammation management.
However, it is important to note that due to the potential toxic and hazardous nature of 2-(dimethylamino)-1,4-diphenylbutane-1,4-dione, strict safety measures and precautions should be taken when handling and using 2-(dimethylamino)-1,4-diphenylbutane-1,4-dione in both laboratory and industrial environments.
Check Digit Verification of cas no
The CAS Registry Mumber 5428-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5428-58:
(6*5)+(5*4)+(4*2)+(3*8)+(2*5)+(1*8)=100
100 % 10 = 0
So 5428-58-0 is a valid CAS Registry Number.
5428-58-0Relevant academic research and scientific papers
Synthesis of tritium labelled 4P-PDOT, a selective melatonin receptor antagonist
Rhee, Sung W.,Tanga, Mary J.
, p. 925 - 932 (2007/10/03)
A selective MT2 melatonin receptor antagonist, 4-phenyl-2-propionamidotetralin (4P-PDOT), was prepared as a tritium-labelled compound with high specific activity and radiochemical purity. Catalytic hydrogenation of a unique vinyl bromo precursor 10 was us
Base Catalysed Rearrangements involving Ylide Intermediates. Part 2. The Stevens and Sigmatropyc Rearrangements of Allylic Ammonium Ylides
Jemison, Robert W.,Laird, Trevor,Ollis, W. David,Sutherland, Ian O.
, p. 1450 - 1457 (2007/10/02)
The base catalysed rearrangements of the quaternary ammonium salts (9) usually gives the sigmatropic rearrangement product (10) rather than the Stevens rearrangement product (11).An earlier claim has been corrected: the corresponding reaction
