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2-Cyclohexen-1-one, 3-hydroxy-5,5-dimethyl-2-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61908-09-6

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61908-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61908-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,0 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61908-09:
(7*6)+(6*1)+(5*9)+(4*0)+(3*8)+(2*0)+(1*9)=126
126 % 10 = 6
So 61908-09-6 is a valid CAS Registry Number.

61908-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-5,5-dimethyl-2-phenylsulfanylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Phenylsulfenyldimedon

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:61908-09-6 SDS

61908-09-6Downstream Products

61908-09-6Relevant academic research and scientific papers

CuI-catalyzed thioarylation of active methylene compounds with in situ generated benzenethiols: Preparation of α-thioaryl-β-dicarbonyls and 4-thioaryl-5-pyrazolones

Golzar, Nooshin,Nowrouzi, Najmeh,Abbasi, Mohammad

, p. 4837 - 4845 (2018)

In this paper, a one-step copper-catalyzed procedure for oxidative coupling of active methylene compounds including cyclic β-diketones, cyclic β-ketoesters and 5-pyrazolone with benzenethiols is described. Benzenethiols are in situ generated in the reaction mixture from aryl halides and thiourea as sulfur transfer reagent. α-Thioaryl compounds are obtained in excellent yields and in short reaction time via the process which is free from the foul smell of thiols.

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