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1-Methoxy-2-(methylselanyl)benzene is an organic compound characterized by a benzene ring with a methoxy group (-OCH3) at the 1-position and a methylselanyl group (-CH2SeH) at the 2-position. 1-methoxy-2-(methylselanyl)benzene is a derivative of anisole, where the hydrogen atom at the 2-position is replaced by a methylselanyl group. The presence of the selenium atom in the molecule imparts unique chemical and physical properties, such as increased lipophilicity and potential reactivity with electrophilic reagents. The compound may have applications in the synthesis of more complex organoselenium compounds, as well as in the study of selenium-containing natural products and pharmaceuticals.

1657-75-6

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1657-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1657-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1657-75:
(6*1)+(5*6)+(4*5)+(3*7)+(2*7)+(1*5)=96
96 % 10 = 6
So 1657-75-6 is a valid CAS Registry Number.

1657-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-2-methylselanylbenzene

1.2 Other means of identification

Product number -
Other names 1-methoxy-2-methylselanyl-benzene

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

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More Details:1657-75-6 SDS

1657-75-6Relevant 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, Properties, and Multinuclear (1H, 13C, 77Se) Magnetic Resonance Studies of the Hybrid Selenide Ligands o-C6H4(SeMe)Y (Y=NMe2, PMe2, AsMe2, SbMe2, OMe, and SMe)

Hope, Eric G.,Kemmitt, Tim,Levason, William

, p. 487 - 490 (2007/10/02)

The reaction of o-bromophenyl methyl selenide with lithium dimethyl-phosphide, -arsenide, and -antimonide gave the seleno-phosphine o-C6H4(SeMe)PMe2 (2), -arsine o-C6H4(SeMe)AsMe2 (3), and -stibine o-C6H4(SeMe)SbMe2 (4) respectively.The seleno-amine o-C6H

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