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1-Pentanone, 1-phenyl-2-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67886-38-8

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67886-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67886-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,8 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67886-38:
(7*6)+(6*7)+(5*8)+(4*8)+(3*6)+(2*3)+(1*8)=188
188 % 10 = 8
So 67886-38-8 is a valid CAS Registry Number.

67886-38-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Phenyl-2-phenylsulfonyl-1-pentanon

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67886-38-8 SDS

67886-38-8Relevant academic research and scientific papers

Oxidative Sulfonylation of Hydrazones Enabled by Synergistic Copper/Silver Catalysis

Xu, Jun,Shen, Chao,Qin, Xian,Wu, Jie,Zhang, Pengfei,Liu, Xiaogang

, p. 3706 - 3720 (2021/02/05)

A copper/silver-cocatalyzed protocol for oxidative sulfonylation of hydrazones is demonstrated. A wide range of β-ketosulfones and N-acylsulfonamides are directly synthesized in moderate to good yields. Our work provides a viable method for scalable preparation of β-ketosulfone derivatives that have found wide applications in the pharmaceutical industry.

NBS-mediated synthesis of β-keto sulfones from benzyl alcohols and sodium arenesulfinates

Muneeswara, Madithedu,Sundaravelu, Nallappan,Sekar, Govindasamy

, p. 3479 - 3484 (2019/05/21)

An efficient synthetic route towards the synthesis of β-keto sulfones has been developed from secondary benzyl alcohols using N-bromosuccinimide (NBS). The present protocol utilizes NBS as oxidant as well as brominating agent, readily accessible benzyl alcohols and sodium arenesulfinates as the sulfonylating reagent under mild conditions. The control experiments revealed that the reaction proceeds via oxidation of alcohol to ketone, α-bromination of ketone and nucleophilic substitution by sodium arenesulfinate. Furthermore, the efficiency of the methodology was tested with a gram scale reaction and also shown the synthetic utility.

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