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1-Methoxy-3-(methylselanyl)benzene is an organic compound characterized by a benzene ring with a methoxy group at the 1st position and a methylselanyl group at the 3rd position. The methoxy group consists of an oxygen atom bonded to a methyl group, while the methylselanyl group is a selenium-containing functional group with a methyl group attached to a selenium atom. 1-methoxy-3-(methylselanyl)benzene is a member of the class of organoselenium compounds, which are known for their diverse applications in various fields, including pharmaceuticals, agrochemicals, and materials science. The presence of selenium in the molecule can confer unique chemical and biological properties, making 1-methoxy-3-(methylselanyl)benzene a potentially interesting compound for further study and development.

2726-42-3

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2726-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2726-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2726-42:
(6*2)+(5*7)+(4*2)+(3*6)+(2*4)+(1*2)=83
83 % 10 = 3
So 2726-42-3 is a valid CAS Registry Number.

2726-42-3SDS

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-methoxy-3-methylselanylbenzene

1.2 Other means of identification

Product number -
Other names m-methylselenoanisole

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:2726-42-3 SDS

2726-42-3Relevant academic research and scientific papers

An electrochemical method for deborylative selenylation of arylboronic acids under metal- and oxidant-free conditions

Cai, Hu,Fu, Zhengjiang,Guo, Shengmei,He, Dongdong,Yi, Xuezheng,Yin, Jian

supporting information, p. 130 - 135 (2022/01/19)

An efficient protocol to synthesize aryl selenoethers through deborylative selenylation of widely available arylboronic acids has been established under electrochemical conditions in the absence of metal catalyst and external oxidant. The synthesis of bio

SYNTHESIS, STRUCTURE, AND PROPERTIES OF COMPOUNDS WITH A CHALCOGEN-NITROGEN BOND. V. N-TRIFLUOROACETYL-Se-ARYL-Se-METHYLSELENIMIDES

Naddaka, V. I.,Krasnov, V. P.,Minkin, V. I.

, p. 432 - 436 (2007/10/02)

The IR and UV spectra of a series of N-trifluoroacetyl-Se-aryl-Se-methylselenimides were studied.The molecules of these compounds, like those of N-acylsulfimides and N-acyltelurimides with similar structures, have a bipolar structure, in which the negative charge is distributed through the bond system of the N-trifluoroacetyl group.

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