36268-76-5 Usage
Uses
Used in Pharmaceutical Synthesis:
Phenyl 4-bromo-1-hydroxynaphthalene-2-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals. Its complex structure allows for the creation of new drug molecules with potential therapeutic properties.
Used in Organic Chemistry:
In the field of organic chemistry, phenyl 4-bromo-1-hydroxynaphthalene-2-carboxylate is employed as a building block for the construction of more complex molecules. Its reactivity and structural features make it a useful component in the synthesis of a wide range of organic compounds.
Used in Medicinal Chemistry Research:
Phenyl 4-bromo-1-hydroxynaphthalene-2-carboxylate is used as a research tool in medicinal chemistry. Its potential biological activity and pharmacological applications are of great interest to scientists, who study its interactions with biological systems to develop new therapeutic strategies.
Used in Drug Development:
Due to its potential pharmacological applications, phenyl 4-bromo-1-hydroxynaphthalene-2-carboxylate is used in the development of new drugs. Its unique structure may contribute to the discovery of novel therapeutic agents with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 36268-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,6 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36268-76:
(7*3)+(6*6)+(5*2)+(4*6)+(3*8)+(2*7)+(1*6)=135
135 % 10 = 5
So 36268-76-5 is a valid CAS Registry Number.
36268-76-5Relevant academic research and scientific papers
Directed Reactions of C-Sulfenyl Halides with 1-Hydroxynaphthalene Derivatives
Movchan,Ziganshina,Akhmetov,Dykhal,Chmutova
, p. 502 - 509 (2007/10/03)
C-Sulfenyl chlorides react with 1-hydroxynaphthalene derivatives in nitrobenzene with the formation of sulfenylation products sulfenylation. Under the same conditions C-sulfenyl bromides furnish the products of bromination. In the presence of potassium perchlorate the reactions occurs place also in dioxane and acetonitrile with retention of different in reactivity patterns of isostructural chlorides and bromides. In the reaction with 1-hydroxynaphthalene 2-nitro- and 2,4-dinitrobenzenesulfenylbromides both afford the bromination and sulfenylation products in unsimilar ratios.
