91632-23-4

Basic information

• Product Name: Benzeneacetic acid, 4-broMo-.alpha.-forMyl-, ethyl ester
• Synonyms: Benzeneacetic acid, 4-broMo-.alpha.-forMyl-, ethyl ester
• CAS NO: 91632-23-4
• Molecular Formula: C₁₁H₁₁BrO₃
• Molecular Weight: 271.10724
• Mol File: 91632-23-4.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzeneacetic acid, 4-broMo-.alpha.-forMyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, 4-broMo-.alpha.-forMyl-, ethyl ester(91632-23-4)
• EPA Substance Registry System: Benzeneacetic acid, 4-broMo-.alpha.-forMyl-, ethyl ester(91632-23-4)

Safety Data

• Hazardous Substances Data: 91632-23-4(Hazardous Substances Data)

Usage

General Description

Benzeneacetic acid, 4-bromo-alpha-formyl-, ethyl ester is a chemical compound that is commonly used in research and industrial applications. It is known for its role as a versatile building block in organic synthesis, where it is often employed in the creation of complex molecules. Benzeneacetic acid, 4-broMo-.alpha.-forMyl-, ethyl ester possesses a bromine atom and a formyl group, making it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Due to its potential reactivity and versatility, it is important to handle this compound with care and in accordance with safety guidelines.

Upstream product

• 14062-25-0 Ethyl 4-bromophenylacetate 
• 109-94-4 formic acid ethyl ester 
• 623-73-4 diazoacetic acid ethyl ester 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 104920-81-2 7-amino-3-(4-bromophenyl)-2-hydroxy-1,8-naphthyridine 
• 104309-70-8 ethyl 3-(4-bromophenyl)-6-methyl-2-oxo-2H-pyran-5-carboxylate 
• 104309-66-2 3-(p-bromophenyl)-6-methyl-2-pyrone 
• 91670-46-1 4-(4-Bromo-phenyl)-2H-isoxazol-5-one 
• 104920-89-0 8-amino-4-(4-bromophenyl)tetrazolo<1,5-a><1,8>naphthyridine 
• 104920-92-5 8-hydroxy-4-(4-bromophenyl)tetrazolo<1,5-a><1,8>naphthyridine 
• 104949-90-8 7-acetamido-2-chloro-3-(4-bromophenyl)-1,8-naphthyridine 
• 104920-83-4 7-acetamido-3-(4-bromophenyl)-2-hydroxy-1,8-naphthyridine 
• 104920-86-7 8-acetamido-4-(4-bromophenyl)tetrazolo<1,5-a><1,8>naphthyridine 
• 104309-68-4 4-(6-Methyl-2-oxo-2H-pyran-3-yl)-benzonitrile 
• 1352442-41-1 3-(4-bromophenyl)-5,7-dimethoxyquinolin-4(1H)-one 
• 91632-41-6 2,5-Bis-(4-bromo-phenyl)-[1,3]oxazin-6-one 
• 91632-48-3 (Z)-3-(4-Bromo-benzoylamino)-2-(4-bromo-phenyl)-acrylic acid 
• 91632-54-1 (Z)-2-(4-Bromo-phenyl)-3-{[1-(4-bromo-phenyl)-1-cyano-meth-(Z)-ylidene]-amino}-acrylic acid 

Relevant articles and documents

Synthesis and anticancer evaluation of 3-substituted quinolin-4-ones and 2,3-dihydroquinolin-4-ones

A series of 3-aryl-5,7-dimethoxyquinolin-4-ones 8 and 3-aryl-5,7-dimethoxy- 2,3-dihydroquinolin-4-ones 13 were synthesized in good yields. Demethylation under a range of conditions afforded the corresponding 5-hydroxy and 5,7-dihydroxy derivatives. Biolog

Synthesis and in vitro evaluation of 3H-pyrrolo[3,2-f]-quinolin-9-one derivatives that show potent and selective anti-leukemic activity

A series of new substituted 7-phenyl-3H-pyrrolo[3,2-f]quinolin-9-ones were synthesized and evaluated for their antiproliferative activity. The most active derivatives showed high selectivity against human leukemia cell lines and potently inhibited their g

Discovery of isoxazolinone antibacterial agents. Nitrogen as a replacement for the stereogenic center found in oxazolidinone antibacterials

A series of potential antimicrobial derivatives possessing bioisosteric replacements for the central oxazolidinone ring found in oxazolidinone antibacterials have been prepared. The design concept involved replacement of the requisite sp3-hybridized stereogenic center found at the 5-position of the oxazolidinone with a nitrogen atom. The synthesis and antibacterial activity of three such ring systems, the benzisoxazolinones, pyrroles, and isoxazolinones is described.