Welcome to LookChem.com Sign In|Join Free
  • or
Bis(3-(trifluoromethyl)phenyl)methanone oxime is a chemical compound with the molecular formula C15H8F6NO. It is a derivative of bis(3-(trifluoromethyl)phenyl)methanone, featuring an oxime functional group. bis(3-(trifluoromethyl)phenyl)methanone oxime is characterized by its two trifluoromethylphenyl groups attached to a central carbonyl group, with the oxime group bonded to the carbonyl carbon. It is an organic molecule that can be used in various chemical reactions and synthesis processes, particularly in the preparation of pharmaceuticals and agrochemicals. The presence of the trifluoromethyl group enhances the compound's lipophilicity and metabolic stability, which can be beneficial in drug design.

2647-39-4

Post Buying Request

2647-39-4 Suppliers

Recommended suppliers

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

2647-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2647-39-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2647-39:
(6*2)+(5*6)+(4*4)+(3*7)+(2*3)+(1*9)=94
94 % 10 = 4
So 2647-39-4 is a valid CAS Registry Number.

2647-39-4Downstream Products

2647-39-4Relevant academic research and scientific papers

Pt-catalyzed O-silylation of oximes by tri-substituted organosilanes

Bhatt, Shreeja V.,Bhatt, Shreya V.,Fotie, Jean

supporting information, p. 1636 - 1639 (2019/06/04)

Silylated derivatives of oximes are important intermediates in organic synthesis, and have found application in the preparation of various nitrogen containing compounds including nitriles, amines, nitrones, and hydroxylamines. An efficient method for the

Visible-Light-Photosensitized Aryl and Alkyl Decarboxylative Functionalization Reactions

Patra, Tuhin,Mukherjee, Satobhisha,Ma, Jiajia,Strieth-Kalthoff, Felix,Glorius, Frank

supporting information, p. 10514 - 10520 (2019/07/12)

Despite significant progress in aliphatic decarboxylation, an efficient and general protocol for radical aromatic decarboxylation has lagged far behind. Herein, we describe a general strategy for rapid access to both aryl and alkyl radicals by photosensitized decarboxylation of the corresponding carboxylic acids esters followed by their successive use in divergent carbon–heteroatom and carbon–carbon bond-forming reactions. Identification of a suitable activator for carboxylic acids is the key to bypass a competing single-electron-transfer mechanism and “switch on” an energy-transfer-mediated homolysis of unsymmetrical σ-bonds for a concerted fragmentation/decarboxylation process.

Palladium-catalyzed annulation of acyloximes with arynes (or alkynes): Synthesis of phenanthridines and isoquinolines

Gerfaud, Thibaud,Neuville, Luc,Zhu, Jieping

supporting information; experimental part, p. 572 - 577 (2009/04/14)

(Chemical Equation Presented) Intermolecular insertion: A palladium-catalyzed domino aminopalladation/C-H functionalization sequence has been developed, and provides access to functionalized phenanthridines and isoquinolines (see scheme; Tf = triflate, TM

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 2647-39-4