Welcome to LookChem.com Sign In|Join Free

CAS

  • or

16271-33-3

Post Buying Request

16271-33-3 Suppliers

Recommended suppliersmore

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

16271-33-3 Usage

Chemical Properties

white to light beige crystalline powder

Uses

2,4-Dichlorobenzenesulfonyl chloride may be used in the preparation of 2,4-dichlorothiophenol.

General Description

2,4-Dichlorobenzenesulfonyl chloride, also known as 2,4-dichlorophenylsulfonyl chloride, is an aryl sulfonyl chloride derivative. It participates in the synthesis of hexahydropyrazino[1,2-a]pyrimidine derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 16271-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,7 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16271-33:
(7*1)+(6*6)+(5*2)+(4*7)+(3*1)+(2*3)+(1*3)=93
93 % 10 = 3
So 16271-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl3O2S/c7-4-1-2-6(5(8)3-4)12(9,10)11/h1-3H

16271-33-3 Well-known Company Product Price

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

  • (A11259)  2,4-Dichlorobenzenesulfonyl chloride, 98%   

  • 16271-33-3

  • 5g

  • 883.0CNY

  • Detail
  • Alfa Aesar

  • (A11259)  2,4-Dichlorobenzenesulfonyl chloride, 98%   

  • 16271-33-3

  • 25g

  • 3704.0CNY

  • Detail
  • Alfa Aesar

  • (A11259)  2,4-Dichlorobenzenesulfonyl chloride, 98%   

  • 16271-33-3

  • 100g

  • 12595.0CNY

  • Detail
  • Aldrich

  • (545694)  2,4-Dichlorobenzenesulfonylchloride  97%

  • 16271-33-3

  • 545694-1G

  • 349.83CNY

  • Detail
  • Aldrich

  • (545694)  2,4-Dichlorobenzenesulfonylchloride  97%

  • 16271-33-3

  • 545694-5G

  • 948.87CNY

  • Detail

16271-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dichlorobenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names Benzenesulfonyl chloride,2,4-dichloro

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:16271-33-3 SDS

16271-33-3Relevant articles and documents

Low-temperature continuous reactor and working method for producing diazo compounds

-

Paragraph 0025-0028; 0038-0042, (2021/03/24)

The invention provides a low-temperature continuous reactor and a working method for producing diazo compounds. The low-temperature continuous reactor comprises two reaction bottles and an overflow kettle, the output end of a first reaction bottle is connected with the input end of a peristaltic pump, and the output end of a second reaction bottle is connected with the input end of a plunger pump;and the input end of the peristaltic pump and the input end of the plunger pump are connected with the overflow kettle in series. Arylamine is used as a starting raw material, a solvent is used for preparing a solution or a uniform mixture, the solution or the uniform mixture and a sodium nitrite solution are continuously fed in a small-volume overflow kettle reactor through a pump for an equivalent reaction, the reacted material is continuously introduced into an acetic acid solution of sulfur dioxide through an overflow pipeline, and through extraction and concentration, the product is obtained, and the total yield is up to 80% or above.

Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists

-

, (2008/06/13)

The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.

Sulfonyl chloride as a disposable electron withdrawing substituent in halex fluorinations

Kageyama, Hiroyuki,Suzuki, Hiroshi,Kimura, Yoshikazu

, p. 85 - 89 (2007/10/03)

Syntheses of 1,3-difluorobenzene and 2,6-difluorotoluene are described via chlorosulfonation, catalytic Halex-fluorination, and desulfination of 1,3-dichlorobenzene and 2,6-dichlorotoluene.

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

What can I do for you?
Get Best Price

Get Best Price for 16271-33-3