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Benzofuran, 2,3-dihydro-7-methyl-2-[(phenylseleno)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71098-92-5

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71098-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71098-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,9 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71098-92:
(7*7)+(6*1)+(5*0)+(4*9)+(3*8)+(2*9)+(1*2)=135
135 % 10 = 5
So 71098-92-5 is a valid CAS Registry Number.

71098-92-5SDS

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 7-methyl-2-(phenylselanylmethyl)-2,3-dihydro-1-benzofuran

1.2 Other means of identification

Product number -
Other names 7-methyl-2-phenylselanylmethyl-2,3-dihydrobenzofuran

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:71098-92-5 SDS

71098-92-5Relevant academic research and scientific papers

Formation of Electrophilic Selenium Species (PhSe+) by Photo-oxidative (Single-electron Transfer) Cleavage of Diphenyl Diselenide

Pandey, G.,Rao, V. Jayathirtha,Bhalerao, U. T.

, p. 416 - 417 (2007/10/02)

Photosensitized (single-electron transfer) cleavage of diphenyl diselenide to give electrophilic selenium species (PhSe+) is reported.

N-PHENYLSELENOPHTHALIMIDE (NPSP) A VALUABLE SELENENYLATING AGENT

Nicolaou, K. C.,Petasis, N. A.,Claremon, D. A.

, p. 4835 - 4842 (2007/10/02)

The phenylseleno group (PhSe) has evolved in recent years as a very useful and versatile functionality.Its facile introduction into organic molecules and its subsequent oxidative or reductive removal, has allowed many important synthetic transformations.D

ORGANOSELENIUM-INDUCED CYCLIZATIONS IN ORGANIC SYNTHESIS

Nicolaou, K.C.

, p. 4097 - 4109 (2007/10/02)

A number of organoselenium reagents are introduced as efficient initiators of ring closures leading from unsaturated substrates to lactones, cyclic ethers, cyclic thioethers, N-heterocycles and carbocycles.These cyclizations often proceed with high ring selectivity and stereoselectivity and are accompained by the incorporation of the phenylseleno group (PheSe) into the final product.Methods are described for the effective removal of this group (PheSe) by oxidation or reduction achieving unsaturation or saturation.Finally the successful application of this Se-based methodology to the synthesis of stable and biologically active prostacyclins is outlined.Representative experimental procedures are included.

Phenylselenoetherification. A Highly Efficient Cyclization Process for the Synthesis of O- and S-Heterocycles

Nicolaou, K. C.,Magolda, R. L.,Sipio, W. J.,Barnette, W. E.,Lysenko, Z.,Joullie, M. M.

, p. 3784 - 3793 (2007/10/02)

Phenylselenoetherification, a new cyclization procedure based on organoselenium chemistry, is described in detail.Unsaturated hydroxy and thio compounds were subjected to this new cyclization process to afford a series of phenyl selenoethers and phenyl selenothioethers which were transformed to a variety of heterocyclic systems by reductive or oxidative removal of the selenium group.Applications to the synthesis of muscarine analogues are described.

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