22366-66-1 Usage
Description
3-bromoThiochroman-4-one, a brominated thiochroman derivative, is a chemical compound characterized by the molecular formula C9H7BrOS. It features a heterocyclic ring with a sulfur atom, and the incorporation of a bromine atom imparts unique chemical and biological properties to this compound. Its distinctive structure and reactivity suggest potential pharmaceutical applications, making it a promising candidate for further research and development in the field of medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
3-bromoThiochroman-4-one is used as a pharmaceutical intermediate for its potential to be developed into new drugs. Its unique structure and reactivity may contribute to the discovery of novel therapeutic agents, particularly in the areas of medicinal chemistry where its properties can be harnessed to address specific health challenges.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 3-bromoThiochroman-4-one serves as a valuable research compound. It is utilized for exploring its chemical properties, understanding its interactions with biological systems, and potentially identifying new mechanisms of action that could lead to the development of innovative pharmaceuticals.
Used in Drug Design and Synthesis:
3-bromoThiochroman-4-one is employed as a key component in the design and synthesis of new drugs. Its unique structural features make it a candidate for the creation of molecules with specific therapeutic targets, potentially leading to more effective treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 22366-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,6 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22366-66:
(7*2)+(6*2)+(5*3)+(4*6)+(3*6)+(2*6)+(1*6)=101
101 % 10 = 1
So 22366-66-1 is a valid CAS Registry Number.
22366-66-1Relevant articles and documents
Base-induced coupling of α-azido ketones with aldehydes -an easy and efficient route to trifunctionalized synthons 2-azido-3-hydroxy ketones, 2-acylaziridines, and 2-acylspiroaziridines
Patonay, Tamas,Juhasz-Toth, Eva,Benyei, Attila
, p. 285 - 295 (2007/10/03)
An improved synthesis of a-azido ketones under phase-transfer conditions has been developed. The transformation of α-azido ketones into acyclic and heterocyclic 2-azido-3-hydroxy ketones has been demonstrated and the relative configurations of the chroman
