1196474-68-6

Basic information

• Product Name: ethyl 4-(3-broMo-4-forMylphenoxy)benzoate
• Synonyms: ethyl 4-(3-broMo-4-forMylphenoxy)benzoate
• CAS NO: 1196474-68-6
• Molecular Formula: C₁₆H₁₃BrO₄
• Molecular Weight: 349.17602
• Mol File: 1196474-68-6.mol

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: ethyl 4-(3-broMo-4-forMylphenoxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-(3-broMo-4-forMylphenoxy)benzoate(1196474-68-6)
• EPA Substance Registry System: ethyl 4-(3-broMo-4-forMylphenoxy)benzoate(1196474-68-6)

Safety Data

• Hazardous Substances Data: 1196474-68-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Manufacturing:
Ethyl 4-(3-bromo-4-formylphenoxy)benzoate is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Production:
Ethyl 4-(3-broMo-4-forMylphenoxy)benzoate is utilized in the production of agrochemicals, where it serves as a key intermediate in the creation of various agricultural chemicals that can enhance crop protection and yield.
Used in Organic Compound Synthesis:
Due to its versatile reactivity, Ethyl 4-(3-bromo-4-formylphenoxy)benzoate is used as a building block in the synthesis of a wide range of organic compounds, contributing to the diversity of chemical products available for various applications.
Used in Specialty Chemicals Production:
It is employed as an intermediate in the production of dyes, pigments, and other specialty chemicals, where its unique properties can enhance the performance and characteristics of these products.
Used in Drug Discovery and Development:
Ethyl 4-(3-bromo-4-formylphenoxy)benzoate has potential applications in drug discovery and development, where its unique chemical structure can be leveraged to create novel therapeutic agents with specific targets and mechanisms of action.

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 59142-68-6 2-bromo-4-fluorobenzaldehyde 

Downstream Products

• 1196474-69-7 ethyl 4-(4-formyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)benzoate 
• 1196473-44-5 ethyl 4-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yloxy)benzoate 
• 1196473-94-5 4-(1-Hydroxy-3-(nitromethyl)-1,3-dihydrobenzo[c][1,2]oxaborol-6-yloxy)benzoic acid 
• 1196473-95-6 ethyl 4-(1-hydroxy-3-(nitromethyl)-1,3-dihydrobenzo[c][1,2]oxaborol-6-yloxy)benzoate 

Relevant articles and documents

Synthesis and SAR of novel benzoxaboroles as a new class of β-lactamase inhibitors

A new class of benzoxaborole β-lactamase inhibitors were designed and synthesized. 6-Aryloxy benzoxaborole 22 inhibited AmpC P99 and CMY-2 with K i values in the low nanomolar range. Compound 22 restored antibacterial activity of ceftazidime against Enterobacter cloacae P99 expressing AmpC, a class C β-lactamase enzyme. The SAR around the arylbenzoxaboroles, which included the influence of linker and substitutions was also established.

BORON-CONTAINING SMALL MOLECULES

This invention relates to, among other items, 6-substituted benzoxaborole compounds and their use for treating bacterial infections.