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Benzene, 1-methyl-3-(methylseleno)-, also known as 1-methyl-3-(methylseleno)benzene or 3-(methylseleno)toluene, is an organoselenium compound with the chemical formula C8H10Se. It is a colorless liquid at room temperature and is characterized by the presence of a benzene ring with a methyl group at the 1st position and a methylseleno group (a selenium-containing analog of a methyl group) at the 3rd position. Benzene, 1-methyl-3-(methylseleno)- is of interest in organic chemistry and materials science due to its unique properties, such as its potential applications in the synthesis of more complex organoselenium compounds and its use as a precursor in the development of new materials with specific electronic or optical properties.

1528-87-6

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1528-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1528-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1528-87:
(6*1)+(5*5)+(4*2)+(3*8)+(2*8)+(1*7)=86
86 % 10 = 6
So 1528-87-6 is a valid CAS Registry Number.

1528-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-methylselanylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-methyl-3-(methylseleno)

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:1528-87-6 SDS

1528-87-6Relevant academic research and scientific papers

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.

Methyl Transfers. 10. The Marcus Equation Application to Soft Nucleophiles

Lewis, Edward S.,McLaughlin, Mark L.,Douglas, Thomas A.

, p. 6668 - 6673 (2007/10/02)

The Marcus equation to methyl transfers is shown to cover reactions of " soft" nucleophiles, although small discrepancies occur.Rates and equilibria are reported for a series of reactions of arylmethylselenides with (p-chlorophenyl)dimethylselenonium ion.Experimental reaction rates between "hard" methylating agents and "soft" nucleophiles show small deviations from the calculated values, mostly but not always in the direction predicted by the HSAB principle.The Marcus equation fails to explain the previously reported "inversion" of reaction rates of 4-nitrothiophenoxide and of 4-nitrophenoxide with methyl iodide and dimethyl sulfate.Identity rates for dimethyl sulfate, methyl methanesulfonate (using 3He), methyl iodide (using 125I), and methyl triflate (using 35S) in sulfolane are reported.

SYNTHESE NOUVELLE ET RAPIDE D'AKYLSELENO ET ALKYLTELLUROARENES AU MOYEN D'ETHERS-COURONNES

Luxen, Andre,Christiaens, Leon

, p. 3905 - 3908 (2007/10/02)

A phase transfer catalytic synthesis of alkylseleno and alkyltelluroarenes is describe from arenediazonium tetrafluoroborates and dialkyldichalcogenides.

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