53590-63-9 Usage
Uses
Used in Pharmaceutical Synthesis:
(7-Bromo-1H-indol-2-yl)Methanol is used as a key intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Its unique structural features make it a valuable building block for creating diverse organic compounds with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (7-Bromo-1H-indol-2-yl)Methanol serves as a promising candidate for drug development. Its potential biological activities and structural properties allow researchers to explore its use in designing new drugs with improved efficacy and selectivity.
Used in Organic Synthesis:
(7-Bromo-1H-indol-2-yl)Methanol is utilized as a reagent in various chemical reactions, contributing to the synthesis of a wide range of organic compounds. Its versatility in organic synthesis makes it an essential component in the development of novel chemical entities and materials.
Used in Drug Development:
(7-Bromo-1H-indol-2-yl)Methanol plays a crucial role in drug development, as its structural features and potential biological activities can be harnessed to create new therapeutic agents. Researchers can leverage (7-BroMo-1H-indol-2-yl)Methanol to design and optimize drug candidates with enhanced pharmacological properties and reduced side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 53590-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,9 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53590-63:
(7*5)+(6*3)+(5*5)+(4*9)+(3*0)+(2*6)+(1*3)=129
129 % 10 = 9
So 53590-63-9 is a valid CAS Registry Number.
53590-63-9Relevant academic research and scientific papers
Facile Synthesis of 3-Halobenzo-heterocyclic-2-carbonyl Compounds via in situ Halogenation-Oxidation
Jiang, Xiaojian,Yang, Junjie,Zhang, Feng,Yu, Pei,Yi, Peng,Sun, Yewei,Wang, Yuqiang
supporting information, p. 2678 - 2683 (2016/09/03)
A facile method to synthesize 3-halobenzo-heterocyclic-2-carbonyl compounds is described. Mechanistic studies suggested that a halo-cyclization process, which generated the unstable spiro-acetal transition state and readily convertible to the corresponding carbonyl compound might be involved. Diverse 3-halobenzo-heterocyclic-2-carbonyl compounds could be synthesized with up to 95 % yield in mild conditions with inexpensive starting materials. (Figure presented.).
