31558-40-4

Basic information

• Product Name: 4-BROMO-3,5-DIMETHOXYBENZALDEHYDE
• Synonyms: 4-BROMO-3,5-DIMETHOXYBENZALDEHYDE;Name: 4-Bromo-3,5-dimethoxybenzaldehyde;4-BROMO-3,5-DIMETHOXYBENZALDEHYDE 97%;3,5-Dimethoxy-4-bromobenzaldehyde;Benzaldehyde, 4-bromo-3,5-dimethoxy-
• CAS NO: 31558-40-4
• Molecular Formula: C₉H₉BrO₃
• Molecular Weight: 245.07
• EINECS: 250-698-8
• Product Categories: Chemical intermediate for Brodimoprim;Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Aromatics;Intermediates;Miscellaneous Reagents
• Mol File: 31558-40-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: 110-111°C
• Boiling Point: 336.6 °C at 760 mmHg
• Flash Point: 157.4 °C
• Appearance: /
• Density: 1.482 g/cm³
• Vapor Pressure: 0.000111mmHg at 25°C
• Refractive Index: 1.567
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 4-BROMO-3,5-DIMETHOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-3,5-DIMETHOXYBENZALDEHYDE(31558-40-4)
• EPA Substance Registry System: 4-BROMO-3,5-DIMETHOXYBENZALDEHYDE(31558-40-4)

Safety Data

• Hazard Codes: Xn,T:
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 31558-40-4(Hazardous Substances Data)

Usage

Description

4-BROMO-3,5-DIMETHOXYBENZALDEHYDE is an organic compound characterized by the presence of a bromo atom at the 4-position, and methoxy groups at the 3 and 5 positions on a benzene ring. It is a fundamental chemical building block used in the synthesis of more complex structures.

Uses

Used in Pharmaceutical Industry:
4-BROMO-3,5-DIMETHOXYBENZALDEHYDE is used as a key intermediate in the synthesis of various pharmaceutical compounds, including drugs with potential therapeutic applications.
Used in Chemical Synthesis:
4-BROMO-3,5-DIMETHOXYBENZALDEHYDE is used as a chemical building block for the synthesis of more complex organic molecules, such as dyes, fragrances, and other specialty chemicals.
Used in Research and Development:
4-BROMO-3,5-DIMETHOXYBENZALDEHYDE is used as a research compound in the development of new chemical reactions and synthetic pathways, contributing to the advancement of organic chemistry and related fields.

InChI:InChI=1/C9H9BrO3/c1-12-7-3-6(5-11)4-8(13-2)9(7)10/h3-5H,1-2H3

Upstream product

• 16534-12-6 3,5-dihydroxy-4-bromobenzoic acid 
• 61367-62-2 (4-bromo-3,5-dimethoxyphenyl)methanol 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 56518-42-4 4-bromo-3,5-dimethoxybenzoic acid 

Downstream Products

• 31558-32-4 (+/-)-1-(4-bromo-3,5-dimethoxyphenyl)-2-nitropropene 
• 344396-19-6 3,5-dimethoxy-4-(1-methylethyl)benzaldehyde 
• 78025-99-7 3,5-dimethoxy-4-ethylbenzaldehyde 
• 56518-41-3 brodimoprim 

Relevant articles and documents

Anti-inflammatory and psoriasis treatment and protein kinase inhibition by hydroxy stilbenes and novel stilbene derivatives and analogues

The present invention provides novel diphenyl ethene compounds and pharmaceutically-acceptable salts thereof. Also provided are methods for making the compounds of the invention as well as methods for the use thereof in the treatment of immune, inflammatory, and auto-immune diseases.

The synthesis of 4-halogen-substituted analogs of trimethoprim

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