1235403-62-9 Usage
Description
4-(2-(3-amino-1H-pyrazol-4-yl)-4-chlorophenoxy)-5-chloro-2-fluoro-N-(thiazol-4-yl)benzenesulfonamide, with a molecular weight of 500.35, is a complex organic compound characterized by its unique chemical structure. It is a derivative of benzenesulfonamide, featuring a pyrazol-4-yl and thiazol-4-yl group, as well as chloro and fluoro substitutions. 4-(2-(3-amino-1H-pyrazol-4-yl)-4-chlorophenoxy)-5-chloro-2-fluoro-N-(thiazol-4-yl)benzenesulfonamide
Molecular Weight: 500.35 has potential applications in various fields due to its distinct chemical properties and interactions.
Uses
Used in Pharmaceutical Industry:
4-(2-(3-amino-1H-pyrazol-4-yl)-4-chlorophenoxy)-5-chloro-2-fluoro-N-(thiazol-4-yl)benzenesulfonamide, Molecular Weight: 500.35, is used as a potential therapeutic agent for targeting specific biological pathways. Its unique chemical structure allows it to interact with various proteins and enzymes, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Chemical Research:
In the field of chemical research, this compound can be utilized as a starting material or a building block for the synthesis of more complex molecules with specific properties and applications. Its unique structure and functional groups make it an interesting subject for further investigation and modification to explore its potential in various chemical reactions and processes.
Used in Material Science:
The distinct chemical structure and properties of 4-(2-(3-amino-1H-pyrazol-4-yl)-4-chlorophenoxy)-5-chloro-2-fluoro-N-(thiazol-4-yl)benzenesulfonamide, Molecular Weight: 500.35, may also find applications in material science. It could be used to develop new materials with specific properties, such as improved stability, reactivity, or selectivity, which can be beneficial in various industrial applications.
References
Alexandrou et al. (2016), ?Subtype-Selective Small Molecule Inhibitors Reveal a Fundamental Role for Nav1.7 in Nociceptor Electrogenesis, Axonal Conduction and Presynaptic Release; PLoS One, 11 e0152405
Theile et al. (2016), The Selective Nav1.7 Inhibitor, PF-05089771, Interacts Equivalently with Fast and Slow Inactivated Nav1.7 Channels; Mol. Pharmacol., 90 540
Swain et al. (2017), Discovery of Clinical Candidate 4-[2-(5-Amino-1H-pyrazol-4-yl)-4-chlorophenoxy]-5-chloro-2-fluoro-N-1,3-thiazol-4-ylbenzenesulfonamide (PF-05089771): Design and Optimization of Diaryl Ether Aryl Sulfonamides as Selective Inhibitors of Na(V)1.7; J. Med. Chem., 60 7029
Check Digit Verification of cas no
The CAS Registry Mumber 1235403-62-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,4,0 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1235403-62:
(9*1)+(8*2)+(7*3)+(6*5)+(5*4)+(4*0)+(3*3)+(2*6)+(1*2)=119
119 % 10 = 9
So 1235403-62-9 is a valid CAS Registry Number.
1235403-62-9Relevant articles and documents
Cycloalkyl-substituted mesyl benzamide derivatives, and preparation method and medical application thereof
-
, (2017/08/25)
The invention relates to cycloalkyl-substitutedmesyl benzamide derivatives, and a preparation method and medical application thereof. The invention particularly discloses compounds disclosed as Formula (I) or pharmaceutically acceptable salts, stereoisomers, solvated compounds or prodrugs thereof, and a preparation method and application thereof. All the groups in the formula are defined in the specification.
