915712-34-4

Basic information

• Product Name: (E)-Ethyl 2-(4-bromophenylimino)acetate
• Synonyms: (E)-Ethyl 2-(4-bromophenylimino)acetate;ethyl(E)-2-((4-bromophenyl)imino)acetate
• CAS NO: 915712-34-4
• Molecular Formula: C₁₀H₁₀BrNO₂
• Molecular Weight: 256.1
• Mol File: 915712-34-4.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-Ethyl 2-(4-bromophenylimino)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-Ethyl 2-(4-bromophenylimino)acetate(915712-34-4)
• EPA Substance Registry System: (E)-Ethyl 2-(4-bromophenylimino)acetate(915712-34-4)

Safety Data

• Hazardous Substances Data: 915712-34-4(Hazardous Substances Data)

Usage

Description

(E)-ethyl 2-(4-bromophenylimino)acetate, also known as ethyl (E)-2-(4-bromophenylimino)acetate, is an organic compound characterized by its chemical formula C11H12BrNO2. This light yellow liquid possesses a molecular weight of 277.12 g/mol and is recognized for its potential applications across various industries due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
(E)-ethyl 2-(4-bromophenylimino)acetate is utilized as an intermediate in the production of pharmaceuticals, playing a crucial role in the synthesis of various medicinal compounds. Its unique structure allows it to be a key component in developing new drugs and improving existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, (E)-ethyl 2-(4-bromophenylimino)acetate serves as an intermediate, contributing to the development of pesticides, herbicides, and other agricultural chemicals. Its incorporation aids in enhancing the effectiveness and selectivity of these products.
Used in Dye Industry:
(E)-ethyl 2-(4-bromophenylimino)acetate is also employed in the dye industry, where it acts as an intermediate for the synthesis of various dyes. Its chemical properties enable the creation of dyes with specific characteristics, such as colorfastness and stability.
Used in Organic Synthesis:
As a reagent in organic synthesis, (E)-ethyl 2-(4-bromophenylimino)acetate is used to facilitate a range of chemical reactions, leading to the formation of diverse organic compounds. Its versatility in this context is highly valued in the field of organic chemistry.
Used in Medicinal Research:
Due to its potential biological activity, (E)-ethyl 2-(4-bromophenylimino)acetate is of interest in medicinal research. Researchers explore its properties to understand its possible applications in the development of new therapeutic agents and treatments.
Used as a Building Block:
(E)-ethyl 2-(4-bromophenylimino)acetate is also used as a building block for the preparation of various other compounds. Its unique structure makes it a valuable component in the synthesis of complex organic molecules for a wide range of applications.

Upstream product

• 924-44-7 glyoxylic acid ethyl ester 
• 106-40-1 4-bromo-aniline 
• 6911-87-1 4-bromo-N-methylaniline 
• 109-94-4 formic acid ethyl ester 
• 2521-92-8 ethyl 2-((4-bromophenyl)amino)acetate 

Downstream Products

• 1134156-24-3 C₃₃H₃₆BrNO₄ 
• 1134156-39-0 C₃₃H₃₆BrNO₄ 
• 1097223-10-3 ethyl 1,3-bis(4-bromophenyl)-4-((4-bromophenyl)amino)-5-oxoimidazolidine-2-carboxylate 
• 1097223-11-4 C₂₆H₂₆Br₃N₃O₄ 
• 22289-05-0 3-methyleneheptane-2,6-dione 
• 1158957-80-2 ethyl 6'-bromo-4',4'-diphenyl-2',4'-dihydro-1'H-spiro[cyclopropane-1,3'-quinoline]-2'-carboxylate 
• 1158957-83-5 ethyl 6'-bromo-4',4'-bis(4-methoxyphenyl)-2',4'-dihydro-1'H-spiro[cyclopropane-1,3'-quinoline]-2'-carboxylate 
• 1169412-43-4 ethyl 6'-bromo-4',4'-bis(4-chlorophenyl)-2',4'-dihydro-1'H-spiro[cyclopropane-1,3'-quinoline]-2'-carboxylate 
• 1158957-81-3 ethyl 6'-bromo-4',4'-di-p-tolyl-2',4'-dihydro-1'H-spiro[cyclopropane-1,3'-quinoline]-2'-carboxylate 
• 1158957-84-6 ethyl 6'-bromo-4'-(4-methoxyphenyl)-4'-phenyl-2',4'-dihydro-1'H-spiro[cyclopropane-1,3'-quinoline]-2'-carboxylate 
• 1169412-44-5 ethyl 6'-bromo-4'-(4-chlorophenyl)-4'-phenyl-2',4'-dihydro-1'H-spiro[cyclopropane-1,3'-quinoline]-2'-carboxylate 
• 1158957-82-4 ethyl 6'-bromo-4',4'-bis(4-fluorophenyl)-2',4'-dihydro-1'H-spiro[cyclopropane-1,3'-quinoline]-2'-carboxylate 
• 1186321-38-9 ethyl 1,3-bis(4-bromophenyl)-4-methyl-5-oxoimidazolidine-2-carboxylate 
• 1330785-21-1 ethyl 2-benzamido-2-(4-bromophenylamino)acetate 

Relevant articles and documents

Multicomponent Approach to Hydantoins and Thiohydantoins Involving a Deep Eutectic Solvent

We report an efficient synthetic strategy to diverse hydantoins and thiohydantoins involving a three-component reaction with the aid of deep eutectic solvent. Here, N,N′-dimethyl urea and N,N′-dimethyl thiourea play a dual role as reactant and reaction medium along with l-(+)-tartaric acid. The three-component reaction provides an easy access to 5-amino-1,3-dialkyl-substituted hydantoins and thiohydantoins in good yields.

Polarity-Reversed Addition of Enol Ethers to Imines under Visible Light: Redox-Neutral Access to Azide-Containing Amino Acids

A three-component and polarity-reversed addition cascade with a glyoxylate-based imine, an enol ether, and TMSN3 was established for the construction of γ-azido amino acids under visible light. This transformation features mild and redox-neutra

Synthesis of Dihydrophenanthridines and Oxoimidazolidines from Anilines and Ethylglyoxylate via Aza Diels-Alder Reaction of Arynes and KF-Induced Annulation

The transition-metal-free multicomponent coupling of arynes, anilines, and ethylglyoxylate, proceeding via an inverse electron-demand aza Diels-Alder cycloaddition and N-arylation, has been demonstrated. This protocol allows rapid access to N-aryl dihydrophenanthridine derivatives in moderate to high yields at room temperature from readily available starting materials. In addition, an unprecedented fluoride induced annulation of ethyl(arylimino)acetates led to the formation of highly functionalized oxoimidazolidine derivatives in good yields under mild conditions.