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2H-Pyran, tetrahydro-2,2-dimethyl-3-(phenylseleno)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114524-29-7

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114524-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114524-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,2 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114524-29:
(8*1)+(7*1)+(6*4)+(5*5)+(4*2)+(3*4)+(2*2)+(1*9)=97
97 % 10 = 7
So 114524-29-7 is a valid CAS Registry Number.

114524-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-3-phenylselanyloxane

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:114524-29-7 SDS

114524-29-7Downstream Products

114524-29-7Relevant academic research and scientific papers

Studies of the reactions of some benzenalkenyl ethers with benzenselenenyl halides

Bugar?i?, Zorica,Konstantinovi?, Stanimir,Mojsilovi?, Biljana

, p. 728 - 731 (2007/10/03)

Intramolecular cyclization of some benzenalkenyl ethers with benzenselenenyl halides (PhSeX, X=Cl and Br) at different temperatures (- 78°C, 0°C and room temperature) has been investigated. It has been found that Δ4-alkenyl benzyl ethers. affor

Electrochemical cyclization of unsaturated hydroxy compounds. Phenylselenoetherification and phenylselenolactonization

Vukicevic,Konstantinovic,Mihailovic

, p. 859 - 865 (2007/10/02)

Phenylselenoetherification and phenylselenolactonization were performed in one step by electrolysis of unsaturated alcohols or carboxylic acids and diphenyl diselenide in organic solvent containing halide ions as mediators.

ELECTROCHEMICAL CYCLIZATION OF UNSATURATED HYDROXY COMPOUNDS. PART I. PHENYLSELENOETHERIFICATION

Mihailovic, M. Lj.,Konstantinovic, S.,Vukicevic, R.

, p. 4343 - 4346 (2007/10/02)

One-step cyclization of alkenols has been accomplished by electrooxidative phenylselenoetherification.The reaction was performed by electrolysis of unsaturated alcohols and diphenyl diselenide in methylene chloride containing tetraethylammonium bromide.

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