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(E)-N-(4-chlorobenzylidene)-3-methylaniline, also known as Methyl (E)-3-(4-chlorobenzylidene)aniline, is an organic compound with the molecular formula C15H14ClN. It is a yellowish solid that serves as an intermediate in the production of other organic compounds and is commonly used in the synthesis of pharmaceuticals, dyes, and other organic products. (E)-N-(4-chlorobenzylidene)-3-methylaniline is also utilized in organic chemistry research and in the production of fine chemicals.

99484-19-2

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99484-19-2 Usage

Uses

Used in Pharmaceutical Industry:
(E)-N-(4-chlorobenzylidene)-3-methylaniline is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications.
Used in Dye Industry:
(E)-N-(4-chlorobenzylidene)-3-methylaniline is used as a starting material in the production of dyes, playing a crucial role in the creation of a wide range of colorants for various applications.
Used in Organic Chemistry Research:
(E)-N-(4-chlorobenzylidene)-3-methylaniline is employed as a research compound in organic chemistry, aiding scientists in understanding the properties and reactions of similar compounds and potentially leading to new discoveries and innovations.
Used in Fine Chemicals Production:
(E)-N-(4-chlorobenzylidene)-3-methylaniline is used as a building block in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, agriculture, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 99484-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,8 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99484-19:
(7*9)+(6*9)+(5*4)+(4*8)+(3*4)+(2*1)+(1*9)=192
192 % 10 = 2
So 99484-19-2 is a valid CAS Registry Number.

99484-19-2Relevant academic research and scientific papers

Sustainable iron-catalyzed direct imine formation by acceptorless dehydrogenative coupling of alcohols with amines

Jaiswal, Garima,Landge, Vinod G.,Jagadeesan, Dinesh,Balaraman, Ekambaram

supporting information, p. 3232 - 3238 (2016/06/15)

The Acceptorless Dehydrogenative Coupling (ADC) of alcohols with amines is reported using a heterogeneous Fe-catalyst. The reaction operates under mild conditions with the liberation of dihydrogen and water as the byproducts. The developed ADC strategy is simple, efficient, exhibits wide functional group tolerance and can be scaled up. The present catalytic approach possesses a dual role; acting as a catalyst as well as being magnetically separable. The sustainable reuse of a heterogeneous iron catalyst is also shown.

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