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N-[(2E)-but-2-en-1-yl]-4-methylaniline, also known as 4-methyl-N-(2-(2E)-buten-1-yl)aniline or 4-methyl-N-(2-butenyl)aniline, is an organic compound with the chemical formula C11H15N. It is a derivative of aniline, featuring a 4-methyl group and a 2-butenyl group attached to the nitrogen atom. N-[(2E)-but-2-en-1-yl]-4-methylaniline is characterized by its alkenyl side chain, which gives it unique chemical properties and reactivity. It is used in various chemical processes and as an intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. Due to its potential applications and reactivity, it is important to handle N-[(2E)-but-2-en-1-yl]-4-methylaniline with care, following proper safety protocols.

4043-69-0

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4043-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4043-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4043-69:
(6*4)+(5*0)+(4*4)+(3*3)+(2*6)+(1*9)=70
70 % 10 = 0
So 4043-69-0 is a valid CAS Registry Number.

4043-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-but-2-enyl]-4-methylaniline

1.2 Other means of identification

Product number -
Other names N-[(2E)-but-2-en-1-yl]-4-methylaniline

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:4043-69-0 SDS

4043-69-0Downstream Products

4043-69-0Relevant academic research and scientific papers

1H-INDAZOLES AS SYNTHETIC AUXILIARIES FOR THE SYNTHESIS OF SECONDARY AROMATIC AMINES

Saladino, Raffaele,Crestini, Claudia,Nicoletti, Rosario

, p. 567 - 574 (2007/10/02)

Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliares is reported.

Catalytic aminomercuration of olefins in a tandem aminomercuration-deoxymercuration; one-step synthesis of secondary n-arylallylamines from allylalcohols

Barluenga, Jose,Perez-Prieto, Julia,Asensio, Gregorio

, p. 2453 - 2460 (2007/10/02)

Allyl alcohols react with primary aromatic amines and stoichiometric amounts of mercury(II) tetrafluoroborate to give mixtures of mono- and diallyl anilines. However, the use of the tandem aminomercuration-deoxymercuration promoted by catalytic mercury(II) tetrafluoroborate allows to perform regiospecifically the monoallylation reaction with very high yields. A mechanism is proposed to account for the observed results.

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