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
• Article Data: 2

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

General Description

Ethyl 4-(3-bromo-4-formylphenoxy)benzoate is a chemical compound with a molecular formula C16H15BrO4. It is a white to off-white powder that is used in the manufacturing of pharmaceuticals, agrochemicals, and other organic compounds. Ethyl 4-(3-broMo-4-forMylphenoxy)benzoate is a derivative of benzoic acid and is commonly used in the synthesis of various organic molecules due to its versatile reactivity and stability. It is also used as an intermediate in the production of dyes, pigments, and other specialty chemicals. Additionally, it has potential use as a building block in drug discovery and development due to its unique chemical structure and properties. Overall, Ethyl 4-(3-bromo-4-formylphenoxy)benzoate is an important compound with various industrial and research applications.

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 
• 1196473-95-6 ethyl 4-(1-hydroxy-3-(nitromethyl)-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 
• 1196473-44-5 ethyl 4-(1-hydroxy-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.