1421840-44-9 Usage
Description
(R)-N-(1-(5-chloro-2-hydroxyphenyl)ethyl)-4-methylbenzenesulfonamide is a complex organic compound that features a sulfonamide group attached to a substituted benzene ring and a chloro-hydroxyphenyl-ethyl moiety. This chemical is recognized for its potential as a drug candidate in pharmaceutical research, with its structural features suggesting possible anti-inflammatory or antibacterial properties. Further exploration is necessary to determine its full therapeutic potential and applications in treating various medical conditions.
Uses
Used in Pharmaceutical Research:
(R)-N-(1-(5-chloro-2-hydroxyphenyl)ethyl)-4-methylbenzenesulfonamide is used as a potential drug candidate for its possible anti-inflammatory or antibacterial properties. Its unique structure positions it as a candidate for further research and development in the pharmaceutical industry, with the aim of identifying and optimizing its therapeutic applications.
Used in Medical Treatments:
As a potential drug candidate, (R)-N-(1-(5-chloro-2-hydroxyphenyl)ethyl)-4-methylbenzenesulfonamide may be utilized for the treatment of various medical conditions that could benefit from its anti-inflammatory or antibacterial effects. The specific applications would depend on the outcomes of ongoing research and clinical trials, which will provide insights into its safety, efficacy, and optimal use in medical treatments.
Further research and studies are essential to fully understand the potential uses and effects of this compound, ensuring that it can be developed and applied responsibly and effectively in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 1421840-44-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,8,4 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1421840-44:
(9*1)+(8*4)+(7*2)+(6*1)+(5*8)+(4*4)+(3*0)+(2*4)+(1*4)=129
129 % 10 = 9
So 1421840-44-9 is a valid CAS Registry Number.
1421840-44-9Relevant articles and documents
Efficient asymmetric synthesis of structurally diverse p-stereogenic phosphinamides for catalyst design
Han, Zhengxu S.,Zhang, Li,Xu, Yibo,Sieber, Joshua D.,Marsini, Maurice A.,Li, Zhibin,Reeves, Jonathan T.,Fandrick, Keith R.,Patel, Nitinchandra D.,Desrosiers, Jean-Nicolas,Qu, Bo,Chen, Anji,Rudzinski, Diandra M.,Samankumara, Lalith P.,Ma, Shengli,Grinberg, Nelu,Roschangar, Frank,Yee, Nathan K.,Wang, Guijun,Song, Jinhua J.,Senanayake, Chris H.
supporting information, p. 5474 - 5477 (2015/04/27)
The use of chiral phosphinamides is relatively unexplored because of the lack of a general method for the synthesis. Reported herein is the development of a general, efficient, and highly enantioselective method for the synthesis of structurally diverse P-stereogenic phosphinamides. The method relies on nucleophilic substitution of a chiral phosphinate derived from the versatile chiral phosphinyl transfer agent 1,3,2-benzoxazaphosphinine-2-oxide. These chiral phosphinamides were utilized for the first synthesis of readily tunable P-stereogenic Lewis base organocatalysts, which were used successfully for highly enantioselective catalysis.
Design and synthesis of chiral oxathiozinone scaffolds: Efficient synthesis of hindered enantiopure sulfinamides and sulfinyl ketimines
Han, Zhengxu S.,Herbage, Melissa A.,Mangunuru, Hari P. R.,Xu, Yibo,Zhang, Li,Reeves, Jonathan T.,Sieber, Joshua D.,Li, Zhibin,Decroos, Philomen,Zhang, Yongda,Li, Guisheng,Li, Ning,Ma, Shengli,Grinberg, Nelu,Wang, Xiaojun,Goyal, Navneet,Krishnamurthy, Dhileep,Lu, Bruce,Song, Jinhua J.,Wang, Guijun,Senanayake, Chris H.
supporting information, p. 6713 - 6717 (2013/07/26)
Is that S-O? The title scaffolds have a highly active and properly differentiated S-O bond for the efficient synthesis of enantiopure sulfinamides. The method is practical, green, and has the potential to provide an economical commercial process for the synthesis of bulky sulfinamides. Copyright
