1260485-22-0 Usage
Uses
Used in Organic Synthesis:
4H-1-Benzopyran-4-one, 8-broMois employed as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for the formation of a wide range of derivatives, making it a versatile component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4H-1-Benzopyran-4-one, 8-broMois used as a building block for the development of pharmaceutical agents. Its incorporation into drug molecules can potentially enhance their therapeutic properties, such as improving binding affinity to target proteins or modulating pharmacokinetic profiles.
Used in Drug Discovery:
4H-1-Benzopyran-4-one, 8-broMois utilized in drug discovery processes to identify novel compounds with potential therapeutic applications. Its unique structural features and biological activities make it a promising candidate for the development of new drugs, particularly in the areas of cancer, inflammation, and other diseases.
Used in the Study of Structure-Activity Relationships:
In pharmacology and biochemistry, 4H-1-Benzopyran-4-one, 8-broMois used to investigate the relationship between the chemical structure of compounds and their biological activities. Understanding these relationships is crucial for the rational design of more effective and safer drugs.
Used in Pharmaceutical Industry:
4H-1-Benzopyran-4-one, 8-broMois used as a key component in the development of new pharmaceuticals for various therapeutic areas. Its unique properties and potential applications make it an important asset in the creation of innovative treatments for a range of diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1260485-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,4,8 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1260485-22:
(9*1)+(8*2)+(7*6)+(6*0)+(5*4)+(4*8)+(3*5)+(2*2)+(1*2)=140
140 % 10 = 0
So 1260485-22-0 is a valid CAS Registry Number.
1260485-22-0Relevant articles and documents
Silanediol-Catalyzed Chromenone Functionalization
Hardman-Baldwin, Andrea M.,Visco, Michael D.,Wieting, Joshua M.,Stern, Charlotte,Kondo, Shin-Ichi,Mattson, Anita E.
, p. 3766 - 3769 (2016/08/16)
Promising levels of enantiocontrol are observed in the silanediol-catalyzed addition of silyl ketene acetals to benzopyrylium triflates. This rare example of enantioselective, intermolecular chromenone functionalization with carbonyl-containing nucleophiles has potential applications in the synthesis of bioactive chromanones and tetrahydroxanthones.
Efficient synthesis of chromones with alkenyl functionalities by the heck reaction
Patonay, Tams,Vasas, Attila,Kiss-Szikszai, Attila,Silva, Artur M. S.,Cavaleiro, Jos A. S.
, p. 1582 - 1593 (2011/08/04)
The usefulness of the Heck reaction in the field of chromones has been demonstrated. Bromochromones with the halogen atom in their rings A and B were reacted with various terminal alkenes to give hitherto unknown alkenyl-substituted chromones. Reactivity of the substrates was found to markedly depend on the position of the bromine atom. Under phosphine-free conditions using a phase-transfer catalyst additive (tetrabutylammonium bromide), shorter reaction periods and usually higher yields were obtained.
