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24966-39-0

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24966-39-0 Usage

Chemical Properties

yellow crystals or chunks

Check Digit Verification of cas no

The CAS Registry Mumber 24966-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24966-39:
(7*2)+(6*4)+(5*9)+(4*6)+(3*6)+(2*3)+(1*9)=140
140 % 10 = 0
So 24966-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl2S/c7-4-2-1-3-5(8)6(4)9/h1-3,9H/p-1

24966-39-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A12854)  2,6-Dichlorothiophenol, 97%   

  • 24966-39-0

  • 5g

  • 304.0CNY

  • Detail
  • Alfa Aesar

  • (A12854)  2,6-Dichlorothiophenol, 97%   

  • 24966-39-0

  • 25g

  • 1200.0CNY

  • Detail
  • Alfa Aesar

  • (A12854)  2,6-Dichlorothiophenol, 97%   

  • 24966-39-0

  • 100g

  • 3825.0CNY

  • Detail

24966-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichlorobenzenethiol

1.2 Other means of identification

Product number -
Other names 2,6-dichlorobenzene-1-thiol

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:24966-39-0 SDS

24966-39-0Relevant articles and documents

Method for preparing substituted thiophenol and heterocyclic thiophenol by continuous flow reactor

-

Paragraph 0063-0064; 0067-0068, (2019/01/14)

The invention relates to a method for preparing substituted thiophenol and heterocyclic thiophenol by a continuous flow reactor. Phenol and phenol derivatives or heterocyclic phenol are taken as starting materials, and target compounds are prepared by four-step reactions of chlorination, esterification, rearrangement and hydrolysis, wherein the rearrangement reaction is conducted in the continuousflow reactor. According to the method, the reaction is guaranteed by a miniaturized heating device for high-temperature reaction and heat generated by the reaction, the conversion rate and the yieldhigher than those in the conventional reactor are obtained in the short residence time of tens of seconds, relevant side reactions are reduced, meanwhile, fluctuation of temperature and concentrationis avoided in the reaction process, temperature run-away and overheat are avoided, and the reaction process is safe and controllable.

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