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Benzenamine, 2-[(phenylseleno)methyl]-, also known as 2-(phenylseleno)methylbenzeneamine or 2-(phenylseleno)methylaniline, is an organic compound with the chemical formula C13H13NSe. It is a derivative of aniline, where a phenylseleno group (C6H5Se) replaces the hydrogen atom at the 2-position. Benzenamine, 2-[(phenylseleno)methyl]- is characterized by its unique structure, which combines the aromatic properties of benzene with the reactivity of the amine and phenylseleno groups. It is used in various chemical reactions and synthesis processes, particularly in the preparation of pharmaceuticals and other organic compounds. Due to its potential applications and reactivity, it is an important molecule in the field of organic chemistry.

3541-44-4

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3541-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3541-44-4 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 3541-44:
(6*3)+(5*5)+(4*4)+(3*1)+(2*4)+(1*4)=74
74 % 10 = 4
So 3541-44-4 is a valid CAS Registry Number.

3541-44-4SDS

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 2-(phenylselanylmethyl)aniline

1.2 Other means of identification

Product number -
Other names o-Amino-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:3541-44-4 SDS

3541-44-4Downstream Products

3541-44-4Relevant academic research and scientific papers

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

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

, p. 4480 - 4483 (2016)

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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