Welcome to LookChem.com Sign In|Join Free
  • or
1,3,2-Dioxaborolane, 2-(pentafluorophenyl)-, is a cyclic boronate ester derived from pentafluorophenylboronic acid, exhibiting notable Lewis acidity due to its electron-deficient pentafluorophenyl group. Its Lewis acidity has been experimentally assessed using a modified Gutmann method, with results corroborated by DFT calculations, which also revealed conformational diversity in its adducts with triethylphosphine oxide. 1,3,2-Dioxaborolane, 2-(pentafluorophenyl)-'s acceptor number correlates with the O-B-O angle, highlighting the influence of geometric and electronic factors on its reactivity. **Other names:** - 2-(Pentafluorophenyl)-1,3,2-dioxaborolane - Pentafluorophenyl-1,3,2-dioxaborolane - Pentafluorophenylboronic acid cyclic ester (1,3,2-dioxaborolane)

336880-93-4

Post Buying Request

336880-93-4 Suppliers

Recommended suppliers

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

336880-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 336880-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,8,8 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 336880-93:
(8*3)+(7*3)+(6*6)+(5*8)+(4*8)+(3*0)+(2*9)+(1*3)=174
174 % 10 = 4
So 336880-93-4 is a valid CAS Registry Number.

336880-93-4Downstream Products

336880-93-4Relevant academic research and scientific papers

A neutral Gold(III)-Boron transmetalation

Hofer, Manuel,Gomez-Bengoa, Enrique,Nevado, Cristina

, p. 1328 - 1332 (2014)

The occurrence of direct transmetalation between gold(III) and boron species during gold-catalyzed cross-coupling reactions has recently become the subject of intense discussion. In this work, we investigate the transmetalation reaction between discrete, stable gold(III) complexes and boron reagents. Interestingly, electron-rich arylboronic acids remain unreactive under neutral conditions, whereas electron-deficient species undergo transmetalation in a highly efficient manner.

Influence of the diol structure on the Lewis acidity of phenylboronates

Adamczyk-Wozniak, Agnieszka,Jakubczyk, Michal,Jankowski, Piotr,Sporzynski, Andrzej,Urbanski, Piotr M.

, p. 415 - 419 (2013)

A series of cyclic esters of pentafluorophenylboronic acid have been obtained and their Lewis acidity evaluated experimentally by a modified Gutmann method. The results based on 31P NMR measurements were compared with those determined by quantum mechanical calculations at the DFT-VSXC/pcS-2 level of theory. The differences in Lewis acidity are discussed on the basis of electronic and geometric parameters. The calculations revealed that the complexes of investigated esters with Et3PO have multiple conformers of a wide range of calculated 31P NMR shielding constants. Additionally, a correlation between the calculated O-B-O angle of esters and the experimental acceptor number was found. Copyright

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 336880-93-4