470716-52-0 Usage
Description
(4-chlorophenyl)(2,5-difluorobenzyl)sulfane is a sulfane compound characterized by a 4-chlorophenyl group connected to a (2,5-difluorobenzyl) group. As a sulfur analog of organic peroxides, this compound holds potential for various biological and pharmaceutical applications. Its distinctive structure and possible reactivity contribute to its significance in the realms of chemistry and pharmacology, making it a promising candidate for further research and development.
Uses
Used in Pharmaceutical Development:
(4-chlorophenyl)(2,5-difluorobenzyl)sulfane is utilized as a pharmaceutical candidate due to its potential biological activities. Its unique structure allows it to be explored for possible therapeutic applications, including the treatment of various diseases and conditions.
Used as a Chemical Intermediate in Organic Synthesis:
In the field of organic synthesis, (4-chlorophenyl)(2,5-difluorobenzyl)sulfane serves as a valuable chemical intermediate. Its reactivity and structural features make it suitable for use in the synthesis of more complex organic compounds, contributing to the advancement of chemical research and the development of new materials.
Used in Research and Development:
(4-chlorophenyl)(2,5-difluorobenzyl)sulfane is employed as a subject of interest in research and development within the fields of chemistry and pharmacology. Its potential applications and unique properties make it a valuable tool for scientists and researchers working to uncover new knowledge and create innovative solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 470716-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,7,1 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 470716-52:
(8*4)+(7*7)+(6*0)+(5*7)+(4*1)+(3*6)+(2*5)+(1*2)=150
150 % 10 = 0
So 470716-52-0 is a valid CAS Registry Number.
470716-52-0Relevant articles and documents
A practical synthesis of a γ-secretase inhibitor
Scott, Jeremy P.,Lieberman, David R.,Beureux, Olivier M.,Brands, Karel M. J.,Davies, Antony J.,Gibson, Andrew W.,Hammond, Deborah C.,McWilliams, Chris J.,Stewart, Gavin W.,Wilson, Robert D.,Dolling, Ulf-H.
, p. 4149 - 4155 (2008/02/05)
(Chemical Equation Presented) A practical and scaleable synthesis of the γ-secretase inhibitor 1 is reported. The inhibitor consists of a central trisubstituted cyclohexane core with appended propionic acid, 2,5-difluorophenyl, and 4-chlorophenylsulfonyl
HETEROCYCLIC METHYL SULFONE DERIVATIVE
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Page/Page column 15, (2010/11/08)
Provided is a compound capable of inhibiting production or secretion of β amyloid protein. A compound represented by the following formula (1): (wherein, R1 represents a heterocyclic group which may have a substituent, R2 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R3 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R4 represents a hydrogen atom or a C1-6 alkyl group, and X represents -S-,-SO- or -SO2-) an N-oxide or S-oxide thereof; a salt thereof; or a solvate thereof; and a medicament containing any of them.
The new cyclohexylpropionic sulfone
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Page/Page column 12, (2008/06/13)
Novel sulphones of formula I are disclosed: The compounds modulate the processing of amyloid precursor protein by gamma-secretase, and hence are useful in the treatment or prevention of Alzheimer's disease.
