Welcome to LookChem.com Sign In|Join Free
  • or
2,2,2-Trifluor-N-(triphenylphosphoranyliden)-acetamid, also known as trifluoro(triphenylphosphoranylidene)acetamide, is a chemical compound with the molecular formula C20H15F3NOP. It is a derivative of acetamide, featuring a trifluoromethyl group (CF3) and a triphenylphosphoranylidene group (P(C6H5)3). 2,2,2-Trifluor-N-(triphenylphosphoranyliden)-acetamid is of interest in organic chemistry and pharmaceutical research due to its unique structure and potential applications as a reagent or intermediate in the synthesis of various compounds. It is typically synthesized through the reaction of trifluoroacetic acid with triphenylphosphine and a suitable coupling agent. The compound's properties, such as its reactivity and stability, make it a valuable tool in the development of new chemical entities and materials.

1588-26-7

Post Buying Request

1588-26-7 Suppliers

Recommended suppliers

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

1588-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1588-26-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1588-26:
(6*1)+(5*5)+(4*8)+(3*8)+(2*2)+(1*6)=97
97 % 10 = 7
So 1588-26-7 is a valid CAS Registry Number.

1588-26-7Downstream Products

1588-26-7Relevant academic research and scientific papers

First synthesis, structure, and reactivity of (acylimino)triaryl-λ5-bismuthanes stabilized by ortho-substituted aryl ligands

Matano, Yoshihiro,Nomura, Hazumi,Shiro, Motoo,Suzuki, Hitomi

, p. 2580 - 2582 (2008/10/08)

The reactive Bi(V)=N bond in (acylimino)-triaryl-λ5-bismuthanes has been found to be stabilized effectively by ortho-substituted aryl ligands such as o-tolyl, o-anisyl, and mesityl groups. These imino-λ5-bismuthanes, in which the bismuth center possesses a distorted tetrahedral geometry, behave as a nitrene precursor as well as an oxidizing agent, depending on the substrates and conditions.

A convenient synthesis of triphenylphosphine acylimides using N-lithiated triphenylphosphine imide

Cristau,Manginot,Torreilles

, p. 382 - 384 (2007/10/02)

A series of triphenylphosphine acylimides and N-(triphenylphosphoranylidene)carbamates have been readily prepared by direct acylation of the N-lithiated triphenylphosphine imide.

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 1588-26-7