6344-95-2 Usage
Uses
Used in Pharmaceutical Industry:
2,3-dibromo-1-(5-chloro-2-hydroxyphenyl)-3-phenylpropan-1-one is used as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique structure allows for the introduction of specific functional groups, making it a valuable component in the development of new medications.
Used in Organic Synthesis:
In the field of organic synthesis, 2,3-dibromo-1-(5-chloro-2-hydroxyphenyl)-3-phenylpropan-1-one is utilized as a reagent to introduce bromine and chlorine atoms, as well as hydroxyphenyl and phenylpropanone moieties into organic molecules. This capability enhances the compound's applicability in creating a diverse range of chemical products.
Used in Chemical Reactions:
2,3-dibromo-1-(5-chloro-2-hydroxyphenyl)-3-phenylpropan-1-one is also employed as a reagent in various chemical reactions, where it can facilitate the formation of new compounds with desired properties. Its presence in these reactions is crucial for achieving specific outcomes, such as the creation of novel pharmaceutical agents or other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 6344-95-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6344-95:
(6*6)+(5*3)+(4*4)+(3*4)+(2*9)+(1*5)=102
102 % 10 = 2
So 6344-95-2 is a valid CAS Registry Number.
6344-95-2Relevant academic research and scientific papers
Synthesis and biological activities of some new quinoxalines
Basawaraj, Raga,Alvi, Shah Nadeemuddin,Chillargi, Neelavati,Gahininath, Wadikar,Zaheeruddin
, p. 147 - 150 (2013/09/24)
The condensation of 5-chloro-2-hydroxyacetophenone 1 with different substituted aromatic aldehydes in ethanol in presence of strong alkali furnished 1-(2-hydroxy-5-chlorophenyl)-3-aryl propen-1-ones 2a-e. Bromination of compounds 2a-e in acetic acid gave 1-(2-hydroxy-5-chlorophenyl)-3-aryl 2,3-dibromopropan-1-ones 3a-e which upon treatment with o-phenylenediamine in methanol in presence of cone sulphuric acid underwent cyclization and resulted in the formation of quinoxaline derivatives 4ae. Structures of compounds were established on the basis of analytical and spectral studies. Further these compounds were evaluated for their antimicrobial activities and some selected compounds were evaluated for antitubercular activities.
