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2-(2-chlorophenylsulfanyl)-phenylamine is an organic compound with the chemical formula C12H10ClNS. It is a derivative of aniline, where one of the hydrogen atoms on the nitrogen is replaced by a 2-chlorophenylsulfanyl group. 2-(2-chlorophenylsulfanyl)-phenylamine is characterized by the presence of a chlorine atom attached to a phenyl ring, which is connected to another phenyl ring through a sulfur atom. It is a colorless solid with a molecular weight of 239.74 g/mol. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain herbicides and insecticides. Due to its reactivity and the presence of a chlorine atom, it is important to handle 2-(2-chlorophenylsulfanyl)-phenylamine with care, as it may have potential health and environmental impacts.

4726-30-1

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4726-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4726-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4726-30:
(6*4)+(5*7)+(4*2)+(3*6)+(2*3)+(1*0)=91
91 % 10 = 1
So 4726-30-1 is a valid CAS Registry Number.

4726-30-1Relevant academic research and scientific papers

Synthesis of phenothiazines via ligand-free CuI-catalyzed cascade C-S and C-N coupling of aryl ortho-dihalides and ortho-aminobenzenethiols

Dai, Chuan,Sun, Xiaofei,Tu, Xingzhao,Wu, Li,Zhan, Dan,Zeng, Qingle

, p. 5367 - 5369 (2012)

A ligand-free CuI-catalyzed cascade C-S and C-N cross coupling of (hetero)aryl ortho-dihalides and ortho-aminobenzenethiols has been developed, and various phenothiazines were synthesized with excellent regioselectivity. A possible mechanism is proposed for the cascade coupling.

Unexpectedly ligand-free copper-catalyzed C-S cross-coupling of benzothiazole with aryl iodides in aqueous solution

Feng, Yi-Si,Qi, Hong-Xia,Wang, Wei-Cheng,Liang, Yu-Feng,Xu, Hua-Jian

supporting information; experimental part, p. 2914 - 2917 (2012/07/27)

A novel synthetic protocol for 2-aminophenyl sulfide derivatives via the reactions of benzothiazole with aryl iodides was reported for the first time. The reactions were catalyzed by CuCl with tetrabutylammonium hydroxide as the base and water as the solvent without ligand at 50°C or room temperature. A variety of aryl iodides underwent the C-S cross-coupling reaction with benzothiazole to afford smoothly the corresponding products in excellent yield.

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