Welcome to LookChem.com Sign In|Join Free
  • or
1-Ethoxy-4-thiocyanatobenzene is an organic compound with the chemical formula C9H9NS. It is a derivative of benzene, featuring an ethoxy group (C2H5O) attached to the first carbon atom and a thiocyanate group (SCN) attached to the fourth carbon atom. 1-ethoxy-4-thiocyanatobenzene is characterized by its aromatic structure, with the thiocyanate group imparting a distinct chemical reactivity and properties. It is used in various chemical synthesis processes and as an intermediate in the production of pharmaceuticals and agrochemicals. The compound's unique structure allows for a range of applications, including its use as a building block in the creation of more complex molecules.

5286-01-1

Post Buying Request

5286-01-1 Suppliers

Recommended suppliers

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

5286-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5286-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5286-01:
(6*5)+(5*2)+(4*8)+(3*6)+(2*0)+(1*1)=91
91 % 10 = 1
So 5286-01-1 is a valid CAS Registry Number.

5286-01-1Downstream Products

5286-01-1Relevant academic research and scientific papers

Fluorium-Initiated Dealkylative Cyanation of Thioethers to Thiocyanates

Chen, Yang,Qi, Hongyi,Chen, Ning,Ren, Demin,Xu, Jiaxi,Yang, Zhanhui

, p. 9044 - 9050 (2019/08/12)

Thioethers are converted to thiocyanates via fluorium-initiated dealkylative cyanation. Selectfluor is used as the oxidant, and trimethylsilyl cyanide is used as the cyanation reagent. The well-streamlined procedure is user-friendly, operationally simple, and step-economical. The current mechanistic studies show that the sulfur radical cation and cyano radical are both involved. They combine to deliver cyanosulfonium, an intermediate toward thiocyanate after dealkylation. Alternatively, a nucleophilic mechanism is also possible. Our dealkyaltive cyanation is also efficient in synthesizing thiocyanates with strongly electrophilic functionalities.

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 5286-01-1