33567-62-3

Basic information

• Product Name: (2,5-dimethoxyphenyl)acetaldehyde
• CAS NO: 33567-62-3
• Molecular Formula: C₁₀H₁₂O₃
• Molecular Weight: 180.2005
• Mol File: 33567-62-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 289.5°C at 760 mmHg
• Flash Point: 119.7°C
• Density: 1.075g/cm³
• Vapor Pressure: 0.00219mmHg at 25°C
• Refractive Index: 1.5
• CAS DataBase Reference: (2,5-dimethoxyphenyl)acetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (2,5-dimethoxyphenyl)acetaldehyde(33567-62-3)
• EPA Substance Registry System: (2,5-dimethoxyphenyl)acetaldehyde(33567-62-3)

Safety Data

• Hazardous Substances Data: 33567-62-3(Hazardous Substances Data)

Usage

General Description

(2,5-dimethoxyphenyl)acetaldehyde is a chemical compound with the molecular formula C10H12O3. It is a derivative of acetaldehyde with two methoxy substituents attached to the phenyl ring. (2,5-dimethoxyphenyl)acetaldehyde is commonly used in the synthesis of various pharmaceuticals and organic compounds due to its reactivity and ability to participate in a variety of chemical reactions. It is also used as a building block in the production of dyes, fragrances, and other industrial chemicals. Additionally, (2,5-dimethoxyphenyl)acetaldehyde has been studied for its potential biological activities, including its role as a precursor in the synthesis of psychoactive substances. However,

Upstream product

• 33567-56-5 3-(2,5-Dimethoxy-phenyl)-oxirane-2-carboxylic acid methyl ester 
• 6202-39-7 homogentisic acid methyl ester dimethyl ether 
• 7417-19-8 2-(2,5-dimethoxyphenyl)ethanol 
• 19754-22-4 2-allyl-1,4-dimethoxybenzene 
• 1758-25-4 (2,5-dimethoxyphenyl)acetic acid 
• 66469-86-1 ethyl (2,5-dimethoxyphenyl)acetate 
• 150-76-5 4-methoxy-phenol 
• 1201-38-3 2',5'-dimethoxyacetophenone 
• 584-82-7 2-allyl-4-methoxyphenol 
• 13391-35-0 allyl (4-methoxyphenyl) ether 

Downstream Products

• 152093-80-6 5-(2,5-dimethoxyphenyl)-3-penten-2-one 
• 66397-39-5 2-Methyl-3-hydroxy-4-(2',5'-dimethoxyphenyl)-but-1-en 
• 1612882-33-3 C₁₁H₁₆O₃ 
• 1612882-42-4 C₁₁H₁₅IO₂ 
• 1612882-16-2 C₁₇H₁₆O₃S₂ 
• 1259330-61-4 sparstolonin B 
• 1399639-06-5 C₂₀H₂₀N₂O₇S 
• 1356862-37-7 C₂₆H₃₅FN₂O₃ 
• 1088496-58-5 1,1-dibromo-3-(2,5-dimethoxyphenyl)propene 
• 66397-42-0 Ethyl-2.6-dimethyl-8-(2'.5'-dimethoxyphenyl)octa-2E_.6E-dienoat 

Relevant articles and documents

Total synthesis of sparstolonin B via a palladium-catalyzed aldehyde α-arylation

A concise and convergent total synthesis of sparstolonin B was developed. A palladium-catalyzed aldehyde α-arylation was utilized to construct the carbon skeleton of the natural product. A subsequent simple one-pot procedure effected global deprotection and closure of the final two rings via an unusual autoredox mechanism for the conversion of a bis-hydroquinone intermediate to the natural product. The 6 step synthetic sequence was realized in 18% overall yield.

Synthetic and crystallographic studies of a new inhibitor series targeting Bacillus anthracis dihydrofolate reductase

Bacillus anthracis, the causative agent of anthrax, poses a significant biodefense danger. Serious limitations in approved therapeutics and the generation of resistance have produced a compelling need for new therapeutic agents against this organism. Baci

SYNTHESIS OF ERBSTATIN

A simple and convenient synthesis of the tyrosinespecific protein kinase inhibitor, erbstatin (1) from cheap and easily accessible 4-methoxyphenol is described.