149757-20-0 Usage
General Description
2,6-dichloro-4-(pentafluorosulfanyl)aniline, also known as SF5-aniline, is a chemical compound with the molecular formula C6H3Cl2F5N. It contains two chlorine atoms, five fluorine atoms, and one nitrogen atom. The pentafluorosulfanyl group attached to the aniline ring gives the compound unique properties and makes it useful in various applications. SF5-aniline is commonly used in the pharmaceutical industry as an intermediate in the synthesis of other organic compounds. It is also utilized in the development of agrochemicals and advanced materials, and its unique structure and properties make it a valuable building block in the field of organic chemistry. Additionally, SF5-aniline may have potential applications in the field of medicinal chemistry due to its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 149757-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,5 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 149757-20:
(8*1)+(7*4)+(6*9)+(5*7)+(4*5)+(3*7)+(2*2)+(1*0)=170
170 % 10 = 0
So 149757-20-0 is a valid CAS Registry Number.
149757-20-0Relevant articles and documents
Substituted arylpyrazoles
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Page/Page column 76, (2008/06/13)
This invention relates to a range of 1-aryl-4-cyclopropylpyrazoles in which the cyclopropyl ring is substituted at the angular position, and pharmaceutically acceptable salts and solvates thereof, to compositions comprising such compounds, processes to their synthesis and their use as parasiticides.
Synthesis of some arylsulfur pentafluoride pesticides and their relative activities compared to the trifluoromethyl analogues
Crowley, Patrick J.,Mitchell, Glynn,Salmon, Roger,Worthington, Paul A.
, p. 138 - 142 (2007/10/03)
Examples of pesticides containing an arylsulfur pentafluoride group were made and their biological activities compared to the corresponding trifluoromethyl analogues. A phenylsulfur pentafluoride analogue of the insecticide fipronil, screened against a resistant strain of Musca domestica, showed higher activity than the corresponding trifluoromethyl analogue.
