Welcome to LookChem.com Sign In|Join Free
  • or
O,O-di-sec-butyl S-(4-methylphenyl)phosphorothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1616795-40-4

Post Buying Request

1616795-40-4 Suppliers

Recommended suppliers

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

1616795-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1616795-40-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,7,9 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1616795-40:
(9*1)+(8*6)+(7*1)+(6*6)+(5*7)+(4*9)+(3*5)+(2*4)+(1*0)=194
194 % 10 = 4
So 1616795-40-4 is a valid CAS Registry Number.

1616795-40-4Downstream Products

1616795-40-4Relevant academic research and scientific papers

A S-aryl thiophosphate preparation method

-

Paragraph 0053-0057, (2017/01/12)

The invention discloses a preparation method of S-aryl phosphorothioate. The preparation method comprises the following steps of (1) adding a copper catalyst, an aryl sulfonyl chloride and phosphite in an organic solvent, reacting for 12-24 h at a temperature of 60-150 DEG C and cooling to a room temperature to obtain a reaction liquid; and (2) concentrating the reaction liquid, separating and purifying to obtain S-aryl phosphorothioate. According to the preparation method of S-aryl phosphorothioate, a one-pot method is adopted; copper is used as the catalyst; economical and easily available aryl sulfonyl chloride and phosphite are used as the raw materials; and a coupling reaction is carried out directly to generate corresponding S-aryl phosphorothioate, without adding alkali in air. A synthetic system has a relatively wide application scope, is compatible with a plurality of groups such as alkoxy, aryl, halogen and acyloxy. The preparation method provided by the invention is simple in process, convenient for operations and mild in reaction conditions, has a wide substrate range and relatively high yield, and is suitable for popularization and application.

Copper-catalyzed reductive coupling of aryl sulfonyl chlorides with H-phosphonates leading to S-aryl phosphorothioates

Bai, Jie,Cui, Xiuling,Wang, Hui,Wu, Yangjie

supporting information, p. 8860 - 8863 (2014/08/05)

An efficient protocol for copper-catalyzed reductive cross-coupling of aryl sulfonyl chlorides with H-phosphonates has been developed. The various S-aryl phosphorothioates were afforded in up to 86% yield for 20 examples. This protocol features high effic

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 1616795-40-4