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Benzene, 1-nitro-2-[(phenylseleno)methyl]-, also known as 1-nitro-2-(phenylselanylmethyl)benzene, is an organic compound with the molecular formula C13H11NOSe. It is a derivative of benzene, featuring a nitro group at the 1-position and a phenylselanylmethyl group at the 2-position. Benzene, 1-nitro-2-[(phenylseleno)methyl]- is characterized by the presence of a selenium atom bonded to a phenyl group, which is in turn connected to the benzene ring through a methylene bridge. The nitro group adds a strong electron-withdrawing effect, influencing the compound's reactivity and properties. This specific arrangement of functional groups makes it a potentially useful intermediate in the synthesis of various organic compounds, particularly those involving selenium-containing moieties.

3541-43-3

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3541-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3541-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3541-43:
(6*3)+(5*5)+(4*4)+(3*1)+(2*4)+(1*3)=73
73 % 10 = 3
So 3541-43-3 is a valid CAS Registry Number.

3541-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-2-(phenylselanylmethyl)benzene

1.2 Other means of identification

Product number -
Other names o-Nitro-benzyl-phenyl-selenid

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:3541-43-3 SDS

3541-43-3Downstream Products

3541-43-3Relevant academic research and scientific papers

Unusual Application for Phosphonium Salts and Phosphoranes: Synthesis of Chalcogenides

Moura, Igor M. R.,Tranquilino, Arisson,Sátiro, Barbara G.,Silva, Ricardo O.,De Oliveira-Silva, Diogo,Oliveira, Roberta A.,Menezes, Paulo H.

, p. 5954 - 5964 (2021/05/04)

A novel strategy for the synthesis of sulfides and selenides from phosphonium salts and thio- or selenesulfonates, commercially available compounds, is described. When phosphoranes were used in the reaction, different products were obtained. The methodology does not require the use of metals, reactive species, or anhydrous conditions to be performed.

α-Alkylation of tertiary amines by C(sp3)–C(sp3) cross-coupling under redox neutral photocatalysis

Pandey, Ganesh,Tiwari, Sandip Kumar,Singh, Bhawana

supporting information, p. 4480 - 4483 (2016/09/14)

Direct α-alkylation of N-phenyl-tetrahydroisoquinoline with alkyl selenides of desired alkyl chain length and functionality is reported by photoredox catalysis. Construction of hexahydro pyrrolo- and pyrido-isoquinoline scaffolds along with indolines and tetrahydroquinolines is also described by intramolecular C(sp3)–C(sp3) cross-couplings.

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