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"Benzene, [(methylseleno)methyl]-" is an organic compound with the chemical formula C7H8Se. It is a derivative of benzene, where one hydrogen atom is replaced by a (methylseleno)methyl group, which consists of a methyl group (CH3) attached to a selenium atom. Benzene, [(methylseleno)methyl]- is also known as selenoethylbenzene or benzylmethylselenide. It is a colorless liquid with a pungent odor and is used in various chemical reactions and as a reagent in organic synthesis. Due to the presence of selenium, it has potential applications in the field of organoselenium chemistry and may exhibit unique chemical properties compared to its sulfur-containing analogs.

5925-78-0

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5925-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5925-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5925-78:
(6*5)+(5*9)+(4*2)+(3*5)+(2*7)+(1*8)=120
120 % 10 = 0
So 5925-78-0 is a valid CAS Registry Number.

5925-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methylselanylmethylbenzene

1.2 Other means of identification

Product number -
Other names Benzylmethylselenylether

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:5925-78-0 SDS

5925-78-0Relevant academic research and scientific papers

Synthesis of Selenolates from Stannyl and Silyl Alkylselenides

Krief, Alain,Badaoui, Elie,Dumont, Willy

, p. 8521 - 8522 (1993)

Stannyl and silyl alkylselenides have been efficiently transformed to the corresponding alkylselenolates on reaction with butyllithiums.Other conditions proved to be limited.

FeCl3-Diorganyl dichalcogenides promoted cyclization of 2-alkynylanisoles to 3-chalcogen benzo[ b ]furans

Gay, Rafaela M.,Manarin, Flavia,Schneider, Caroline C.,Barancelli, Daniela A.,Costa, Michael D.,Zeni, Gilson

supporting information; experimental part, p. 5701 - 5706 (2010/10/03)

A general synthesis of 3-chalcogen benzo[b]furans from the readily available 2-alkynylanisoles, via FeCl3/diorganyl dichalcogenides intramolecular cyclization, has been developed. Aryl and alkyl groups directly bonded to the chalcogen atom were used as cycling agents. The results revealed that the reaction significantly depends on the electronic effects of substituents in the aromatic ring bonded to the selenium atom of the diselenide species. We observed that the pathway of reaction was not sensitive to the nature of substituents in the aromatic ring of anisole since both the electron-donating and the electron-withdrawing groups delivered the products in similar yields. In addition, the obtained heterocycles were readily transformed to more complex products by using a chalcogen/lithium exchange reaction with n-BuLi followed by trapping of the lithium intermediate with aldehydes, furnishing the desired secondary alcohols in good yields.

Synthesis and molecular structures of dialkylselenonium methylide complexes of indium tribromide

De Andrade, Fabiano Molinos,Massa, Werner,Peppe, Clovis,Uhl, Werner

, p. 1294 - 1299 (2007/10/03)

The reaction of bromomethyl-dibromo-indium(III), Br2InCH 2Br with dialkylselenides, R1SeR2 (R 1 = CH3, R2 = CH2C6H 5; R1 = C2H5, R2 = CH2C6H5; R1 = R2 = CH2C6H5) afforded the corresponding dialkylselenonium methylide complexes of indium tribromide, Br 3InCH2SeR1R2, which were fully characterized by NMR spectroscopy and single crystal X-ray diffraction studies.

Experimental and theoretical studies on the nature of weak nonbonded interactions between divalent selenium and halogen atoms

Iwaoka, Michio,Katsuda, Takayuki,Komatsu, Hiroto,Tomoda, Shuji

, p. 321 - 327 (2007/10/03)

(Chemical Equation Presented). To investigate the nature of weak nonbonded selenium...halogen interactions (Se...X interactions; X = F, Cl, and Br), three types of model compounds [2-(CH2X)C6H 4SeY (1-3), 3-(CH2

Convenient transformation of benzyl alcohol into its corresponding selenide using the selenolate anion-aluminum chloride combination system

Abe, Hitoshi,Yamasaki, Akira,Fujii, Hiroyuki,Harayama, Takashi

, p. 2223 - 2226 (2007/10/03)

Treatment of benzyl alcohol with a new reagent system, benzene- or methaneselenolate anion-aluminum chloride, yielded the corresponding selenide. The one-pot conversion of benzaldehyde into benzyl selenide was also achieved by this system.

Reactions of Dialkyl(aryl) Diselenides with Alkyl(aryl) 2,2-Dichlorovinyl Sulfides under Conditions of Phase-Transfer Catalysis as a Route to Alkyl(aryl)thioacetylenes and 1-Alkyl(aryl)thio-1,2-bis-2-chloroethenes

Martynov, A. V.,Kozyreva, O. B.,Mirskova, A. N.

, p. 469 - 477 (2007/10/03)

Phase-transfer reactions between dialkyl(aryl) diselenides R'SeSeR' and alykl(aryl) 2,2-dichlorovinyl sulfides RSCH=CCl2, catalyzed by benzyltributylammonium chloride and 18-crown-6, yields alkyl(aryl)thioacetylenes RSCCSR', (Z)- and

SELENYLATION OF TRI- AND TETRACHLOROETHYLENE BY ORGANIC DISELENIDES UNDER CONDITIONS OF PHASE-TRANSFER CATALYSIS

Martynov, A. V.,Mirskova, A. N.,Voronkov, M. G.

, p. 1602 - 1608 (2007/10/02)

The selenylation of tetrachloroethylene by organic diselenides under the conditions of phase-transfer catalysis leads to the formation of 1,2-bis(organoseleno)-1,2-dichloroethylenes in 50percent solution of sodium hydroxide and to a mixture of trichlorovi

SYNTHESIS OF SELENOACETALS

Clarembeau, M.,Cravador, A.,Dumont, W.,Hevesi, L,Krief, A.,et al.

, p. 4793 - 4812 (2007/10/02)

This paper reports our results concerning the syntheses of various bis(alkylseleno)alkanes and some of their arylseleno analogues by different methods.The scope and limitation of each of them are presented.

NOVEL SYNTHESIS OF TERTIARY ALKYL, SECONDARY AND TERTIARY BENZYL, AND ALLYL SELENIDES FROM THE CORRESPONDING ALCOHOLS

Clarembeau, M.,Krief, A.

, p. 3625 - 3628 (2007/10/02)

We report an efficient synthesis of the title compounds from alcohols and selenols.The scope and limitations of the new method are disclosed.

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