30091-24-8

Basic information

• Product Name: 2-(ethylamino)benzonitrile
• Synonyms: 2-(ethylamino)benzonitrile
• CAS NO: 30091-24-8
• Molecular Formula: C₉H₁₀N₂
• Molecular Weight: 146.1891
• Mol File: 30091-24-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(ethylamino)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(ethylamino)benzonitrile(30091-24-8)
• EPA Substance Registry System: 2-(ethylamino)benzonitrile(30091-24-8)

Safety Data

• Hazardous Substances Data: 30091-24-8(Hazardous Substances Data)

Usage

General Description

2-(ethylamino)benzonitrile is a chemical compound that consists of a benzene ring with a nitrile group and an ethylamino group attached to it. It is commonly used in the pharmaceutical and agrochemical industries as an intermediate for the synthesis of various organic compounds. This chemical exhibits a variety of potential biological activities, including antimicrobial, antitumor, and antioxidant properties. Additionally, 2-(ethylamino)benzonitrile can also be utilized as a building block for the production of dyes, pigments, and other specialty chemicals. However, it is important to handle this compound with caution due to its toxic and potentially hazardous nature.

Upstream product

• 75-03-6 ethyl iodide 
• 1885-29-6 anthranilic acid nitrile 
• 394-47-8 2-fluorobenzonitrile 
• 802294-64-0 propionic acid 
• 612-64-6 N-ethyl-N-nitrosoaniline 
• 55305-43-6 N-cyano-N-phenyl-p-toluenesulfonamide 

Downstream Products

• 125160-57-8 3-Allyl-1-(2-cyano-phenyl)-1-ethyl-urea 
• 61453-53-0 2-methyl-4-phenylquinazoline 

Relevant articles and documents

Visible-Light-Enabled Direct Decarboxylative N-Alkylation

The development of efficient and selective C?N bond-forming reactions from abundant feedstock chemicals remains a central theme in organic chemistry owing to the key roles of amines in synthesis, drug discovery, and materials science. Herein, we present a dual catalytic system for the N-alkylation of diverse aromatic carbocyclic and heterocyclic amines directly with carboxylic acids, by-passing their preactivation as redox-active esters. The reaction, which is enabled by visible-light-driven, acridine-catalyzed decarboxylation, provides access to N-alkylated secondary and tertiary anilines and N-heterocycles. Additional examples, including double alkylation, the installation of metabolically robust deuterated methyl groups, and tandem ring formation, further demonstrate the potential of the direct decarboxylative alkylation (DDA) reaction.

Method of inhibiting neoplastic cells with imidazoquinazoline derivatives

A method for inhibiting neoplasia, particularly cancerous and precancerous lesions by exposing the affected cells to imidazoquinazoline derivatives.

Cytomegalovirus inhibiting compounds

The present invention relates to heterocyclic compounds having antiviral activity. In particular, compounds of formula (I): wherein B, W, X, Y, R1, R2, R3, R4 and n are as defined herein, are useful in the thera