473299-50-2 Usage
Uses
Used in Pharmaceutical Industry:
[3,5-difluoro-4-(methylthio)phenyl]methanol is used as a key compound in the manufacturing process for various pharmaceuticals. Its unique properties and reactivity contribute to the synthesis of a wide range of biologically active compounds, making it a valuable asset in the development of novel medications.
Used in Agrochemical Industry:
In the agrochemical sector, [3,5-difluoro-4-(methylthio)phenyl]methanol is employed as a vital component in the production of various agrochemicals. Its role in this industry is instrumental in the creation of effective and targeted solutions for agricultural applications.
Used in Organic Synthesis:
[3,5-difluoro-4-(methylthio)phenyl]methanol is used as a chiral reagent in organic synthesis. Its distinctive properties enable it to facilitate the creation of enantiomerically pure compounds, which are essential in various chemical reactions and applications.
Used in Material Science:
[3,5-difluoro-4-(methylthio)phenyl]methanol is also utilized in the field of material science, where it serves as a building block for the development of new materials with specific properties. Its unique structure and reactivity make it a promising candidate for the creation of innovative materials with potential applications in various industries.
Despite its numerous potential applications, it is essential to handle [3,5-difluoro-4-(methylthio)phenyl]methanol with care due to its potential health risks. Proper safety measures and precautions should be taken to minimize any risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 473299-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,2,9 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 473299-50:
(8*4)+(7*7)+(6*3)+(5*2)+(4*9)+(3*9)+(2*5)+(1*0)=182
182 % 10 = 2
So 473299-50-2 is a valid CAS Registry Number.
473299-50-2Relevant academic research and scientific papers
Design of Potent and Orally Active GPR119 Agonists for the Treatment of Type II Diabetes
Liu, Ping,Hu, Zhiyong,Dubois, Byron G.,Moyes, Christopher R.,Hunter, David N.,Zhu, Cheng,Kar, Nam Fung,Zhu, Yuping,Garfunkle, Joie,Kang, Ling,Chicchi, Gary,Ehrhardt, Anka,Woods, Andrea,Seo, Toru,Woods, Morgan,Van Heek, Margaret,Dingley, Karen H.,Pang, Jianmei,Salituro, Gino M.,Powell, Joyce,Terebetski, Jenna L.,Hornak, Viktor,Campeau, Louis-Charles,Lamberson, Joe,Ujjainwalla, Fez,Miller, Michael,Stamford, Andrew,Wood, Harold B.,Kowalski, Timothy,Nargund, Ravi P.,Edmondson, Scott D.
, p. 936 - 941 (2015/08/24)
We report herein the design and synthesis of a series of potent and selective GPR119 agonists. Our objective was to develop a GPR119 agonist with properties that were suitable for fixed-dose combination with a DPP4 inhibitor. Starting from a phenoxy analo
SUBSTITUTED CYCLOPROPYL COMPOUNDS
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, (2014/04/17)
Substituted cyclopropyl piperidinyl compounds and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR-1 19. Pharmaceutical compositions and methods of treatment are also included.
SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT
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, (2013/02/28)
Substituted cyclopropyl compounds of the formula I: and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. The compounds are useful as agonists of the G-protein coupled rece
Fluoro-substituted benzenesulfonyl compounds for the treatment of inflammation
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, (2008/06/13)
Methods of treating cyclooxygenase-2 mediated disorders comprising administering to a subject a therapeutically effective amount of one or more fluoro-substituted benzenesulfonyl compounds corresponding to Formula I: wherein A, X, n, R1, R
