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4-(tert-butyl)phenyl 3-trifluoromethylphenyl sulfide is an organic compound characterized by its molecular formula C15H15F3S. 4-(tert-butyl)phenyl 3-trifluoromethylphenyl sulfide features a phenyl ring with a tert-butyl group (a carbon chain with three methyl groups attached to a central carbon) at the 4-position and another phenyl ring with a trifluoromethyl group (a carbon atom bonded to three fluorine atoms) at the 3-position. The two phenyl rings are connected by a sulfur atom, forming a sulfide bridge. This specific arrangement of functional groups gives the compound unique chemical properties, making it potentially useful in various applications such as pharmaceuticals, agrochemicals, or materials science. The compound's structure and properties can be further explored through its chemical reactivity, stability, and potential interactions with other molecules.

1479-84-1

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1479-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1479-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1479-84:
(6*1)+(5*4)+(4*7)+(3*9)+(2*8)+(1*4)=101
101 % 10 = 1
So 1479-84-1 is a valid CAS Registry Number.

1479-84-1Relevant academic research and scientific papers

CN and CS bond forming cross coupling in water with amphiphilic resin-supported palladium complexes

Hirai, Yoshinori,Uozumi, Yasuhiro

experimental part, p. 934 - 935 (2011/12/05)

Catalytic CN and CS bond forming reactions of haloarenes with secondary amines and benzenethiols were achieved in water under heterogeneous conditions by the use of immobilized palladium complexes coordinated with the amphiphilic polystyrenepoly( ethylene glycol) resin-supported di(tert-butyl)phosphane ligand to afford aryl(dialkyl)amines and diaryl sulfides in high yield.

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