Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Diselenide, bis(pentafluorophenyl), also known as (C6F5)2Se2, is a selenium-based chemical compound characterized by its two pentafluorophenyl groups attached to the selenium atoms. It is known for its reactivity and ability to participate in various organic synthesis reactions, making it a promising candidate for applications in materials science, catalysis, and medicinal chemistry. However, it is important to handle Diselenide, bis(pentafluorophenyl) with caution due to its potential health hazards and toxicity if ingested or inhaled.

18064-78-3

Post Buying Request

18064-78-3 Suppliers

Recommended suppliersmore

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

18064-78-3 Usage

Uses

Used in Chemical Reactions:
Diselenide, bis(pentafluorophenyl) is used as a reagent in various chemical reactions for its ability to participate in organic synthesis processes.
Used in Materials Science:
In the field of materials science, Diselenide, bis(pentafluorophenyl) is utilized for its potential applications in the development of new materials with unique properties.
Used in Catalysis:
Diselenide, bis(pentafluorophenyl) is employed as a catalyst or catalyst precursor in various chemical processes, enhancing the efficiency and selectivity of reactions.
Used in Medicinal Chemistry:
In medicinal chemistry, Diselenide, bis(pentafluorophenyl) is studied for its potential applications in the synthesis of pharmaceutical compounds and the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 18064-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,6 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18064-78:
(7*1)+(6*8)+(5*0)+(4*6)+(3*4)+(2*7)+(1*8)=113
113 % 10 = 3
So 18064-78-3 is a valid CAS Registry Number.

18064-78-3Relevant articles and documents

Diselenide-Mediated Catalytic Functionalization of Hydrophosphoryl Compounds

Handoko,Benslimane, Zacharia,Arora, Paramjit S.

, p. 5811 - 5816 (2020/07/27)

We report a diaryldiselenide catalyst for cross-dehydrogenative nucleophilic functionalization of hydrophosphoryl compounds. The proposed organocatalytic cycle closely resembles the mechanism of the Atherton-Todd reaction, with the catalyst serving as a recyclable analogue of the halogenating agent employed in the named reaction. Phosphorus and selenium NMR studies reveal the existence of a P-Se bond intermediate, and structural analyses indicate a stereospecific reaction.

Synthesis, chemistry, and characterization of perfluoroaromatic selenium derivatives

Klapoetke, Thomas M.,Krumm, Burkhard,Polborn, Kurt

, p. 1359 - 1366 (2007/10/03)

The reaction of perfluoroaryllithium RC6F4Li, where R = F or 4- CF3C6F4O, respectively, with selenium gives the known diselanes (RC6F4Se)2 (1a, 1b). Redox reactions of

Reactions of Monocyclopentadienyl Complexes of Molybdenum and Tungsten with Derivatives of Phenols and Pentafluorobenzeneselenol

Davidson, Jack L.,Holz, Birgit,Leverd, Pascal C.,Lindsell, W. Edward,Simpson, Nigel J.

, p. 3527 - 3532 (2007/10/02)

Reactions of (cp = η5-C5H5) with thallium salts Tl(OR) (R = aryl) in tetrahydrofuran did not produce simple substitution products but afforded reduced species 2, oxidised species or the thalliu

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 18064-78-3