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Benzenamine, 2-[(3-methoxyphenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54815-64-4

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54815-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54815-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,1 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54815-64:
(7*5)+(6*4)+(5*8)+(4*1)+(3*5)+(2*6)+(1*4)=134
134 % 10 = 4
So 54815-64-4 is a valid CAS Registry Number.

54815-64-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxyphenyl)sulfanylaniline

1.2 Other means of identification

Product number -
Other names 2-Aminophenyl-3-methoxyphenylsulfid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54815-64-4 SDS

54815-64-4Downstream Products

54815-64-4Relevant academic research and scientific papers

Heterogeneous copper-catalyzed synthesis of S-arylated 2-aminothiophenols via ring opening of benzothiazoles and C-S coupling using aryl halides

Ichikawa, Tomohiro,Matsuo, Tomohiro,Tachikawa, Takumu,Sawama, Yoshinari,Monguchi, Yasunari,Sajiki, Hironao

, p. 793 - 805 (2019/04/26)

Chelate resins, which are polystyrene-divinylbenezene-based polymers bearing iminodiacetic acids or polyamines as ligands, supported copper catalysts (Cu/CR11 or Cu/CR20) in effectively catalyzing the ring cleaving S-arylation of benzothiazole with aryl i

Metal-Free Iodine-Catalyzed Direct Arylthiation of Substituted Anilines with Thiols

Yang, Daoshan,Yan, Kelu,Wei, Wei,Zhao, Jing,Zhang, Mengqi,Sheng, Xuguang,Li, Guoqing,Lu, Shenglei,Wang, Hua

, p. 6083 - 6092 (2015/06/30)

Iodine-catalyzed direct arylthiation of substituted anilines for the synthesis of various diaryl sulfides has been developed under metal- and solvent-free conditions. The present method uses readily available thiols as the arylthiation reagents, and envir

Iron-catalyzed S-arylation of benzothiazole with aryl iodides under aqueous medium: Facile synthesis of aryl(2-aminoaryl) sulfides

Lee, Hang Wai,Yung, Ka Fu,Kwong, Fuk Yee

supporting information, p. 2743 - 2747 (2015/01/08)

A simple route for facile access of aryl(2-aminoaryl) sulfide was reported. With the aid of iron(III) chloride catalyst and diamine ligand, benzothiazole was efficiently S-arylated with various aryl iodides (19 examples) in water under air atmosphere. This operationally simple protocol provides aryl(2-aminoaryl) sulfides in moderate to good yields.

Iron-Catalyzed S-Arylation of Benzothiazole with Aryl Iodides under Aqueous Medium: Facile Synthesis of Aryl(2-aminoaryl) Sulfides

Lee, Hang Wai,Yung, Ka Fu,Kwong, Fuk Yee

, p. 2743 - 2747 (2015/05/05)

A simple route for facile access of aryl(2-aminoaryl) sulfide was reported. With the aid of iron(III) chloride catalyst and diamine ligand, benzothiazole was efficiently S-arylated with various aryl iodides (19 examples) in water under air atmosphere. This operationally simple protocol provides aryl(2-aminoaryl) sulfides in moderate to good yields.

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