138035-68-4 Usage
Description
5-CHLORO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE is a chemical compound belonging to the oxazine class, characterized by a benzene ring fused to an oxazine ring and a chlorine atom attached to the benzene ring. 5-CHLORO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE holds potential pharmaceutical significance due to its diverse biological activities, such as antimicrobial, antifungal, and anticancer properties. Its unique structure and reactivity contribute to its value as a building block for the synthesis of novel drugs and other biologically active compounds, making it a subject of interest for ongoing research and drug development.
Uses
Used in Pharmaceutical Industry:
5-CHLORO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE is used as a pharmaceutical compound for its antimicrobial properties, serving as a potential agent against various types of infections caused by bacteria and other microorganisms. Its ability to inhibit microbial growth makes it a candidate for the development of new antibiotics and antifungal drugs.
Used in Anticancer Applications:
In the field of oncology, 5-CHLORO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE is used as an anticancer agent, leveraging its potential to target and inhibit the growth of cancer cells. Its diverse pharmacological activities suggest that it could be a promising candidate for the development of novel cancer therapies, particularly for cancers where existing treatments are limited or ineffective.
Used in Drug Synthesis:
5-CHLORO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE is utilized as a key building block in the synthesis of novel drugs and biologically active compounds. Its unique structure and reactivity allow for the creation of new chemical entities with potential therapeutic applications, contributing to the advancement of drug discovery and development.
Used in Research and Development:
In the scientific community, 5-CHLORO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE is used as a subject of interest for further research and drug development. Its diverse range of biological activities and potential pharmaceutical applications make it a valuable compound for exploring new therapeutic strategies and understanding its mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 138035-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,0,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138035-68:
(8*1)+(7*3)+(6*8)+(5*0)+(4*3)+(3*5)+(2*6)+(1*8)=124
124 % 10 = 4
So 138035-68-4 is a valid CAS Registry Number.
138035-68-4Relevant articles and documents
REACTION OF 7-SUBSTITUTED 4-HYDROXYL-1,4-BENZOXAZIN-3-ONES IN STRONGLY ACIDIC MEDIA
Quiroz, Andres,Niemeyer, Hermann M.
, p. 1681 - 1685 (2007/10/02)
Kinetic and product studies of the reaction of 7-substituted 4-hydroxyl-1,4-benzoxazin-3-ones in strongly acidic media produced biphasic Hammett plots which indicated the intermediacy of a highly elctrophilic nitrogen compound with nitrenium ion character.
