58483-28-6 Usage
Uses
Used in Pharmaceutical Industry:
1-(3,5-DICHLORO-2-HYDROXYPHENYL)-3-PHENYLPROPANE-1,3-DIONE is used as an intermediate in the synthesis of pharmaceuticals for its potential to create new compounds with useful properties. The presence of the hydroxyl group and the phenyl group in the molecule allows for further functionalization and modification, which can lead to the development of novel drugs with enhanced therapeutic effects.
Used in Organic Chemistry Research:
In the field of organic chemistry, 1-(3,5-DICHLORO-2-HYDROXYPHENYL)-3-PHENYLPROPANE-1,3-DIONE serves as a valuable compound for research purposes. Its unique structure enables scientists to explore various chemical reactions and mechanisms, contributing to the advancement of organic chemistry knowledge and the discovery of new synthetic pathways.
Used in Biochemistry Applications:
1-(3,5-DICHLORO-2-HYDROXYPHENYL)-3-PHENYLPROPANE-1,3-DIONE is also utilized in biochemistry for studying the interactions between molecules and biological systems. Its structural features make it an interesting candidate for investigating molecular recognition, enzyme inhibition, and other biological processes, potentially leading to the development of new bioactive compounds and a better understanding of biological mechanisms.
Used in Medicinal Chemistry:
In medicinal chemistry, 1-(3,5-DICHLORO-2-HYDROXYPHENYL)-3-PHENYLPROPANE-1,3-DIONE is employed as a key intermediate in the design and synthesis of new drugs. Its structural diversity and the possibility of further modification make it a promising starting point for the development of innovative therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 58483-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,8 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58483-28:
(7*5)+(6*8)+(5*4)+(4*8)+(3*3)+(2*2)+(1*8)=156
156 % 10 = 6
So 58483-28-6 is a valid CAS Registry Number.
58483-28-6Relevant articles and documents
Rh(III)-Catalyzed Aldehydic C?H Functionalization Reaction between Salicylaldehydes and Sulfoxonium Ylides
Xu, Guo-Dong,Huang, Kenneth L.,Huang, Zhi-Zhen
supporting information, p. 3318 - 3323 (2019/06/25)
A novel aldehydic C?H functionalization reaction between salicylaldehydes and sulfoxonium ylides has been developed under rhodium(III) catalysis, affording coupling products in moderate to good yields. A plausible mechanism involving aldehydic C(sp2)?H activation by rhodium(III) and rhodium(III) catalyzed carbene insertion is also proposed. It was also found that the aldehydic C?H functionalization followed by dehydrative cyclization was able to produce flavonoids in one-pot. (Figure presented.).
Synthesis of novel fused chromone-pyrimidine hybrids and 2,4,5-trisubstituted pyrimidine derivatives via ANRORC rearrangement
Sambaiah,Raghavulu,Shiva Kumar,Yennam, Satyanarayana,Behera, Manoranjan
, p. 10020 - 10026 (2017/09/18)
A facile and versatile procedure for the synthesis of functionalized novel 2,5-diphenyl-5H-chromeno[4,3-d]pyrimidin-5-ol and (2,4-diphenylpyrimidin-5-yl) (2-hydroxyphenyl) methanone has been described. The key step in the synthesis involves the ANRORC rea
Synthesis and study of chlorosubstituted 4-aroyl and 4-alkoyl-pyrazolines, pyrazoles and their effect on some flowering plants
Mahale, Jaishree D.,Manoja,Belsare,Rajput
experimental part, p. 505 - 511 (2010/10/20)
Some new chlorosubstituted 4-aroyl/alkoylpyrazolines 5a,b and 4-aroyl/alkoylpyrazoles 7a,b have been synthesized by condensation of 1-(2'-hydroxy-3'-5'-dichlorophenyl)-3-aryl/alkyl-1-3-propanedione 3a,b and valeraldehyde by Baker-Venkatraman transformatio
