1208318-08-4

Basic information

• Product Name: Ethyl 7-(4-broMophenyl)-4,7-dioxoheptanoate
• Synonyms: Ethyl 7-(4-broMophenyl)-4,7-dioxoheptanoate;-4,7-dioxoheptanoate;Ethyl 7-(4-bromophenyl)
• CAS NO: 1208318-08-4
• Molecular Formula: C₁₅H₁₇BrO₄
• Molecular Weight: 341.19708
• Mol File: 1208318-08-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Ethyl 7-(4-broMophenyl)-4,7-dioxoheptanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 7-(4-broMophenyl)-4,7-dioxoheptanoate(1208318-08-4)
• EPA Substance Registry System: Ethyl 7-(4-broMophenyl)-4,7-dioxoheptanoate(1208318-08-4)

Safety Data

• Hazardous Substances Data: 1208318-08-4(Hazardous Substances Data)

Usage

Description

Ethyl 7-(4-bromophenyl)-4,7-dioxoheptanoate is a chemical compound characterized by the molecular formula C13H13BrO4. It is a derivative of ethyl heptanoate, distinguished by the attachment of a 4-bromophenyl group to the seventh carbon atom. Ethyl 7-(4-bromophenyl)-4,7-dioxoheptanoate is recognized for its role in organic synthesis, particularly as a building block in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. The incorporation of the bromophenyl group endows the compound with unique properties and reactivity, which are valuable across various applications in the chemical and pharmaceutical sectors. Safe handling and storage are crucial to mitigate any potential risks associated with this chemical.

Uses

Used in Pharmaceutical Industry:
Ethyl 7-(4-bromophenyl)-4,7-dioxoheptanoate serves as a key intermediate in the synthesis of pharmaceuticals. Its unique structure and reactivity contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 7-(4-bromophenyl)-4,7-dioxoheptanoate is utilized as a precursor in the production of agrochemicals, potentially enhancing crop protection and yield through targeted pest control.
Used in Organic Synthesis:
Ethyl 7-(4-bromophenyl)-4,7-dioxoheptanoate is employed as a building block in organic synthesis for the preparation of a variety of fine chemicals, leveraging its structural features to create complex molecules with specific applications.
Used in Chemical Research:
Ethyl 7-(4-bromophenyl)-4,7-dioxoheptanoate is also used in chemical research to explore novel reactions and mechanisms, further expanding the understanding of organic chemistry and its applications in material science and related fields.

Upstream product

• 132434-53-8 1-(4-bromophenyl)-3-(furan-2-yl)-2-propen-1-one 
• 99-90-1 para-bromoacetophenone 
• 64-17-5 ethanol 
• 98-01-1 furfural 

Downstream Products

• 1208318-55-1 ethyl 4,7-dioxo-7-(4-(2-oxooxazolidin-3-yl)phenyl)heptanoate 
• 1208318-56-2 ethyl 3-(1-(4-carbamoyl-2-methylphenyl)-5-(4-(2-oxooxazolidin-3-yl)phenyl)-1H-pyrrol-2-yl)propanoate 
• 1208316-88-4 3-(1-(4-carbamoyl-2-methylphenyl)-5-(4-(2-oxooxazolidin-3-yl)phenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1208318-48-2 ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate 
• 1208872-51-8 C₂₆H₂₈N₄O₄S 
• 1208316-62-4 3-(5-(4-(2-methyl-1H-imidazol-1-yl)phenyl)-1-(2-methyl-4-(methylsulfonamido)phenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1208316-98-6 3-(1-(4-acetamido-2-methylphenyl)-5-(4-(2-methyl-1H-imidazol-1-yl)phenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1208315-31-4 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-hydroxy-2-methylphenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1208315-93-8 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1366233-23-9 C₂₄H₂₁N₃O₄ 
• 1208316-16-8 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-acetamido-2-methylphenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1208316-20-4 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(2-methyl-4-propionamidophenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1208316-21-5 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(2-methoxyacetamido)-2-methylphenyl)-1H-pyrrol-2-yl)propanoic acid 
• 1208317-72-9 3-(1-(4-hydroxyphenyl)-5-(4-(2-methyl-1H-imidazol-1-yl)phenyl)-1H-pyrrol-2-yl)propanoic acid 

Relevant articles and documents

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The present invention is directed to inhibitors of S-nitrosoglutathione reductase (GSNOR), pharmaceutical compositions comprising such GSNOR inhibitors, and methods of making and using the same.