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N-[2-(phenylthio)phenyl]benzamide is a complex organic chemical compound with the molecular formula C19H15NOS. It is characterized by a benzamide group attached to a phenyl ring, which in turn is connected to another phenyl ring through a sulfur atom. This sulfur atom forms a thiophene bridge, creating a unique structure that distinguishes it from other benzamide derivatives. The compound is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its specific chemical properties and reactivity. Its structure and potential uses make it a subject of interest for researchers in organic chemistry and related disciplines.

3526-11-2

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3526-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3526-11-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3526-11:
(6*3)+(5*5)+(4*2)+(3*6)+(2*1)+(1*1)=72
72 % 10 = 2
So 3526-11-2 is a valid CAS Registry Number.

3526-11-2Relevant academic research and scientific papers

Synthesis of Functionalized Diaryl Sulfides by Cobalt-Catalyzed Coupling between Arylzinc Pivalates and Diaryl Disulfides

Dong, Zhi-Bing,Balkenhohl, Moritz,Tan, Eric,Knochel, Paul

supporting information, p. 7581 - 7584 (2018/11/27)

An efficient protocol for the cobalt-catalyzed preparation of diaryl sulfides from solid organozinc pivalates and commercially available diaryl disulfides is reported. This cross-coupling proceeds at room temperature and displays a good functional group tolerance, allowing the preparation of a diversity of symmetrical or asymmetrical diaryl sulfides in 60-95% yield.

Modified conditions for copper-catalyzed ipso-thiolation of arylboronic acid esters with thiosulfonates

Kanemoto, Kazuya,Yoshida, Suguru,Hosoya, Takamitsu

, p. 85 - 88 (2018/01/26)

An efficient ipso-thiolation of arylboronic acid esters with thiosulfonates has been achieved under mild and odorless conditions using a copper catalyst. The use of TMEDA and cesium fluoride as the ligand and base, respectively, dramatically facilitated the desired transformation. The method exhibited a broad substrate scope, which allowed for the expeditious synthesis of diverse aryl sulfides from easily available starting materials.

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