Welcome to LookChem.com Sign In|Join Free
  • or
1-(phenylsulfonyl)octan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82972-50-7

Post Buying Request

82972-50-7 Suppliers

Recommended suppliers

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

82972-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82972-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,7 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82972-50:
(7*8)+(6*2)+(5*9)+(4*7)+(3*2)+(2*5)+(1*0)=157
157 % 10 = 7
So 82972-50-7 is a valid CAS Registry Number.

82972-50-7Relevant academic research and scientific papers

Synthesis of γ-keto sulfones by copper-catalyzed oxidative sulfonylation of tertiary cyclopropanols

Konik, Yulia A.,Elek, Gábor Zoltán,Kaabel, Sandra,J?rving, Ivar,Lopp, Margus,Kananovich, Dzmitry G.

, p. 8334 - 8340 (2017/10/23)

Tertiary cyclopropanols undergo ring-opening oxidative sulfonylation to afford γ-keto sulfones when reacting with sulfinate salts in the presence of a copper(ii) acetate catalyst and an oxidant (tert-butyl hydroperoxide or atmospheric oxygen). Various fluoroalkyl, aryl and alkyl sulfinate salts are successfully employed as sulfonylation reagents, affording the corresponding sulfones in up to 94% yields. The experimental protocol is mild and tolerates a number of functionalities in the cyclopropanol substrate. The reaction proceeds via a one-pot oxidation-Michael addition mechanism and can serve as a useful addition to the existing methods for the preparation of γ-keto sulfones based on the sulfa-Michael reaction.

Straightforward radical organic chemistry in neat conditions and "on water"

Shapiro, Nelly,Kramer, Maria,Goldberg, Israel,Vigalok, Arkadi

supporting information; experimental part, p. 582 - 584 (2010/09/05)

Radicals generated during aldehyde oxidation to carboxylic acids can be efficiently trapped under environmentally friendly conditions, either in neat conditions or "on water".

Lewis Acid - Mediated Addition of Lithiated Alkyl Phenyl Sulphones and Oxiranes. A Method for Synthesis of α,β-Unsaturated Ketones

Marczak, S.,Wicha, J.

, p. 1511 - 1520 (2007/10/02)

Efficiency of the reaction of lithiated alkyl aryl sulphones (1-4) with oxiranes (5, 6) is increased by the presence of BF3 or CeCl3.The respective adducts (7-14) were transformed into α,β-unsaturated ketones (15-22) with high yields.

1,4-ADDITION REACTION OF NON-ALLYLIC SULFONYL CARBANION WITH CYCLOPENTENONE DERIVATIVE IN THE PRESENCE OF HMPA. SYNTHESIS OF 15-KETO PROSTAGLANDIN F1

Nokami, Junzo,Ono, Toshio,Kurihara, Hideyuki,Wakabayashi, Shoji

, p. 607 - 608 (2007/10/02)

1,4-Addition reaction of aliphatic (non-allylic) sulfonyl carbanion to cyclopentenone was studied to build the vinyl ketone function at the β position of the carbonyl of cyclopentenone. 15-Keto PG F1 (6) was synthesized from sulfone ketal 1 and

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 82972-50-7