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Benzene, 1-methoxy-4-methyl-2-(phenylseleno)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73401-78-2

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73401-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73401-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,0 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73401-78:
(7*7)+(6*3)+(5*4)+(4*0)+(3*1)+(2*7)+(1*8)=112
112 % 10 = 2
So 73401-78-2 is a valid CAS Registry Number.

73401-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-methyl-2-(phenylseleno)benzene

1.2 Other means of identification

Product number -
Other names 1-methoxy-4-methyl-2-phenylselenobenzene

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:73401-78-2 SDS

73401-78-2Downstream Products

73401-78-2Relevant academic research and scientific papers

Peracetic acid mediated sp2 C-H selenation of arenes

Hsieh, Ping-An,Badsara, Satpal Singh,Tsai, Chia-Hsuan,Reddy, Daggula Mallikarjuna,Lee, Chin-Fa

supporting information, p. 1557 - 1562 (2016/06/14)

Peracetic acid promoted C-Se coupling reaction of arenes with diselenides under metal-free and solvent-free conditions has been described. The resulting selenide ethers were obtained in good to excellent yields. Peracetic acid provided the selenide ethers

Catalytic Selenium-Promoted Intermolecular Friedel-Crafts Alkylation with Simple Alkenes

Tang,Zhao, Yinjiao,Li, Wen,Wang, Weilin,Zhang, Meng,Dai, Xin

supporting information, p. 912 - 915 (2016/03/15)

A method for conducting selenium-promoted intermolecular Friedel-Crafts (F-C) alkylation reactions has been developed with simple alkenes using trimethylsilyl trifluoromethanesulfonate as a catalyst and N-phenylselenophthalimide as an efficient selenium s

Relations between 77Se NMR chemical shifts of (phenylseleno)-benzenes and their molecular structures derived from nine X-ray crystal structures

Oddershede, Jette,Henriksen, Lars,Larsen, Sine

, p. 1053 - 1060 (2007/10/03)

An extensive library of 77Se chemical shifts have been generated from the NMR measurements on substituted (phenylseleno)benzenes, including 33 new compounds. The variation in chemical shifts cover 265 ppm ranging from 446 to 181 ppm. Crystal st

Oxidation of Benzylic Hydrocarbons with Benzeneseleninic Anhydride and Related Reactions

Barton, Derek H. R.,Hui, Raymond A. H. F.,Ley, Steven V.

, p. 2179 - 2186 (2007/10/02)

The use of benzeneseleninic anhydride as a new side-chain oxidant for a variety of aromatic and heteroaromatic hydrocarbons has been investigated.The oxidation normally proceeds well for simple substrates, neat or in chlorobenzene solution at 100-130 deg C.In examples where the aromatic rings are susceptible towards electrophilic attack selenated compounds are usually formed as the major by-products.

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