Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, 1-chloro-4-(hexylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59693-91-3

Post Buying Request

59693-91-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

59693-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59693-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,9 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59693-91:
(7*5)+(6*9)+(5*6)+(4*9)+(3*3)+(2*9)+(1*1)=183
183 % 10 = 3
So 59693-91-3 is a valid CAS Registry Number.

59693-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-hexylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-chloro-4-(hexylthio)

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:59693-91-3 SDS

59693-91-3Relevant academic research and scientific papers

Reductive cleavage of S-S bond by Zn/AlCl3 system: A novel method for the synthesis of sulfides from alkyl tosylates and disulfides

Movassagh, Barahman,Mossadegh, Amir

, p. 2337 - 2343 (2007/10/03)

Alkyl and aryl disulfides are reduced by zinc powder in the presence of AlCl3 in aqueous media to yield zinc thiolates. These thiolate anion species then react with alkyl tosylates to give sulfides in high to excellent yields.

Reductive cleavage of S-S bond by Zn/AlCl3 system: A novel method for the synthesis of sulfides from alkyl tosylates and disulfides

Movassagh, Barahman,Mossadegh, Amir

, p. 1685 - 1690 (2007/10/03)

Alkyl and aryl disulfides are reduced by zinc powder in the presence of AlCl3 in aqueous media to yield zinc thiolates. This thiolate anion species then react with alkyl tosylates to give sulfides in high execellent yields.

Synthesis of organic sulfides via Zn/AlCl3 system in aqueous media

Lakouraj,Movassagh,Fadaei

, p. 1237 - 1242 (2007/10/03)

An efficient procedure for preparation of various sulfides has been introduced through a simple reaction of disulfides with suitable alkyl or aryl halides which is promoted by commercial zinc powder in the presence of AlCl3 in aqueous media at 65°C.

Synthesis of organic sulfides from disulfides using a Zn/AlCl3 system in aqueous media

Movassagh,Lakouraj,Fadaei

, p. 350 - 351 (2007/10/03)

A convenient procedure for the synthesis of organic sulfides from different alkyl halides and aryl disulfides by a Zn/AlCl3 system in aqueous media is presented.

Reductive Cleavage of the S-Si Bond in Arylsulfanyltrimethylsilanes: A Novel Method for the Synthesis of Unsymmetrical Sulfides

Zhang, Songtin,Zhang, Yongmin M.

, p. 48 - 49 (2007/10/03)

Arylsulfanyltrimethylsilanes are reduced by samarium diiodide to yield samarium arylthiolates which react with alkyl halides to give unsymmetrical sulfides.

Properties of an (Arylthiomethylene)cyclohexanone

Welzel, Peter,Schmidt, Juergen

, p. 576 - 585 (2007/10/02)

The configuration of 2--6,6-dimethylcyclohexanone (2) and the reactions of 2--6,6-dimethylcyclohexanone (3) with electrophiles have been investigated.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 59693-91-3