81805-97-2

Basic information

• Product Name: 3-BROMO-5-ETHOXY-4-METHOXYBENZALDEHYDE
• Synonyms: 3-bromo-5-ethoxy-4-methoxybenzaldehyde(SALTDATA: FREE)
• CAS NO: 81805-97-2
• Molecular Formula: C₁₀H₁₁BrO₃
• Molecular Weight: 259.11
• Mol File: 81805-97-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 327.6°C at 760 mmHg
• Flash Point: 151.9°C
• Appearance: /
• Density: 1.425g/cm³
• Vapor Pressure: 0.0002mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: 3-BROMO-5-ETHOXY-4-METHOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-5-ETHOXY-4-METHOXYBENZALDEHYDE(81805-97-2)
• EPA Substance Registry System: 3-BROMO-5-ETHOXY-4-METHOXYBENZALDEHYDE(81805-97-2)

Safety Data

• Hazardous Substances Data: 81805-97-2(Hazardous Substances Data)

Usage

Description

3-Bromo-5-ethoxy-4-methoxybenzaldehyde is a chemical compound with the molecular formula C10H11BrO3. It is a derivative of benzaldehyde, featuring bromine, ethoxy, and methoxy substitutes on the benzene ring. 3-BROMO-5-ETHOXY-4-METHOXYBENZALDEHYDE is known for its unique structural properties, making it a valuable intermediate in the synthesis of pharmaceuticals and organic compounds.
Used in Pharmaceutical Industry:
3-Bromo-5-ethoxy-4-methoxybenzaldehyde is used as an intermediate in the synthesis of new drugs for its unique structural properties, contributing to the development of innovative pharmaceuticals.
Used in Organic Synthesis:
3-Bromo-5-ethoxy-4-methoxybenzaldehyde is used as a key component in organic synthesis processes, facilitating the creation of a variety of organic compounds.
Used in Chemical Research:
3-Bromo-5-ethoxy-4-methoxybenzaldehyde is utilized in chemical research to explore its properties and potential applications, furthering the understanding of its role in chemical reactions and compound development.
It is important to handle 3-bromo-5-ethoxy-4-methoxybenzaldehyde with care and store it according to recommended safety guidelines to ensure safe usage and handling.

InChI:InChI=1/C10H11BrO3/c1-3-14-9-5-7(6-12)4-8(11)10(9)13-2/h4-6H,3H2,1-2H3

Upstream product

• 3111-37-3 3-bromo-5-ethoxy-4-hydroxybenzaldehyde 
• 74-88-4 methyl iodide 
• 1131-52-8 3-ethoxy-4-methoxybenzaldehyde 

Downstream Products

• 1207549-13-0 C₂₁H₂₃BrN₂O₆ 
• 90132-51-7 2-(3-Ethoxy-5-ethylsulfanyl-4-methoxy-phenyl)-ethylamine 
• 90132-39-1 2-(3-Ethoxy-4-methoxy-5-methylsulfanyl-phenyl)-ethylamine 
• 90132-44-8 2-[2-(3-Ethoxy-5-ethylsulfanyl-4-methoxy-phenyl)-ethyl]-isoindole-1,3-dione 
• 90132-28-8 1-Ethoxy-3-ethylsulfanyl-2-methoxy-5-((E)-2-nitro-vinyl)-benzene 
• 90132-25-5 1-Ethoxy-2-methoxy-3-methylsulfanyl-5-((E)-2-nitro-vinyl)-benzene 
• 90132-17-5 3-Ethoxy-5-ethylsulfanyl-4-methoxy-benzaldehyde 
• 952017-46-8 1-Ethoxy-3-ethylsulfanyl-5-(2-iodo-ethyl)-2-methoxy-benzene 
• 90132-13-1 3-Ethoxy-4-methoxy-5-methylsulfanyl-benzaldehyde 
• 952017-41-3 1-Ethoxy-3-ethylsulfanyl-2-methoxy-5-vinyl-benzene 
• 75287-20-6 3-ethoxy-4,5-dimethoxybenzaldehyde 
• 81805-96-1 [1-(3-Bromo-5-ethoxy-4-methoxy-phenyl)-meth-(E)-ylidene]-cyclohexyl-amine 

Relevant articles and documents

Solid state nuclear bromination with N-bromosuccinimide. Part 2. Experimental and theoretical studies of reactions with some substituted benzaldehydes

N-Bromosuccinimide reacts with aromatic aldehydes in the solid state to yield exclusively nuclear brominated products while a similar reaction in the solution phase produces a number of products under varied conditions. The reactivity and regioselectivity have been studied in terms of the energies of HOMO, HOMO-LUMO difference, reaction free energy, reaction conditions and crystal packing. Single crystal X-ray structural analysis of 3,4-dihydroxybenzaldehyde has been carried out. Crystal packing energies of some of the reactive and unreactive benzaldehydes indicate the importance of molecular bromine diffusion in the solid state.