87736-79-6 Usage
Description
2,2,2-Trifluoro-1-(4-methylphenyl)-O-[(4-methylphenyl)sulfonyl]oxime ethanone, also known as 2,2,2-Trifluoro-1-(4-methylphenyl)ethanone O-Tosyl Oxime, is a white solid compound with the chemical formula C16H14F3NO2S. It is characterized by the presence of a trifluoromethyl group, a 4-methylphenyl group, and a tosyl (4-methylphenylsulfonyl) group attached to an oxime ether. This unique structure endows it with specific chemical properties that make it valuable in various applications.
Uses
Used in Organic Synthesis:
2,2,2-Trifluoro-1-(4-methylphenyl)-O-[(4-methylphenyl)sulfonyl]oxime ethanone is used as a synthetic intermediate in the chemical industry for the preparation of various organic compounds. Its unique structure allows it to serve as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2,2-Trifluoro-1-(4-methylphenyl)-O-[(4-methylphenyl)sulfonyl]oxime ethanone is used as a key intermediate in the synthesis of drug candidates. Its presence in the molecular structure can impart specific biological activities, such as anti-inflammatory, analgesic, or antipyretic properties, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
2,2,2-Trifluoro-1-(4-methylphenyl)-O-[(4-methylphenyl)sulfonyl]oxime ethanone is also utilized in the agrochemical industry as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. Its unique chemical properties can contribute to the development of more effective and environmentally friendly agrochemical products.
Used in Specialty Chemicals:
In the specialty chemicals sector, 2,2,2-Trifluoro-1-(4-methylphenyl)-O-[(4-methylphenyl)sulfonyl]oxime ethanone is employed as a component in the synthesis of various specialty chemicals, such as dyes, fragrances, and flavoring agents. Its unique structure can provide specific properties that enhance the performance and quality of these specialty products.
Check Digit Verification of cas no
The CAS Registry Mumber 87736-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,3 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87736-79:
(7*8)+(6*7)+(5*7)+(4*3)+(3*6)+(2*7)+(1*9)=186
186 % 10 = 6
So 87736-79-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H14F3NO3S/c1-11-3-7-13(8-4-11)15(16(17,18)19)20-23-24(21,22)14-9-5-12(2)6-10-14/h3-10H,1-2H3/b20-15-
87736-79-6Relevant articles and documents
Photochemical Cyclopropenation of Alkynes with Diazirines as Carbene Precursors in Continuous Flow
Tanbouza, Nour,Carreras, Virginie,Ollevier, Thierry
, p. 5420 - 5424 (2021/07/26)
An efficient synthesis of 3-trifluoromethyl-3-aryl-cyclopropenes via the cyclopropenation reaction of alkynes with photolytically generated carbenes from diazirine compounds is described. This reaction is performed in continuous flow using readily available LEDs under mild reaction conditions. This new and efficient method describes the synthesis of 25 examples of 3-trifluoromethyl-3-aryl-cyclopropenes with yields up to 97%, achieved in continuous flow with a 5 min residence time. Control experiments highlighted that diazirines are more efficient than diazo compounds for this transformation.
Rapid Mapping of Protein Interactions Using Tag-Transfer Photocrosslinkers
Horne, Jim E.,Walko, Martin,Calabrese, Antonio N.,Levenstein, Mark A.,Brockwell, David J.,Kapur, Nikil,Wilson, Andrew J.,Radford, Sheena E.
, p. 16688 - 16692 (2018/11/27)
Analysing protein complexes by chemical crosslinking-mass spectrometry (XL-MS) is limited by the side-chain reactivities and sizes of available crosslinkers, their slow reaction rates, and difficulties in crosslink enrichment, especially for rare, transie
Is Magnetic Bistability of Carbenes a General Phenomenon? Isolation of Simple Aryl(trifluoromethyl)carbenes in Both Their Singlet and Triplet States
Tsegaw, Yetsedaw A.,Kadam, Pritam E.,T?tsch, Niklas,Sanchez-Garcia, Elsa,Sander, Wolfram
, p. 12310 - 12316 (2017/09/12)
p-Tolyl(trifluoromethyl)carbene and the related fluorenyl(trifluoromethyl)carbene were synthesized in solid argon and characterized by IR, UV-vis, and electron paramagnetic resonance spectroscopy as well as by quantum mechanical calculations. The carbenes