6527-32-8

Basic information

• Product Name: 4-(BENZYLOXY)-3,5-DIMETHOXYBENZALDEHYDE
• Synonyms: 3,5-dimethoxy-4-phenylmethoxybenzaldehyde
• CAS NO: 6527-32-8
• Molecular Formula: C₁₆H₁₆O₄
• Molecular Weight: 272.3
• Mol File: 6527-32-8.mol
• Article Data: 53

Chemical Properties

• Melting Point: 63 °C(Solv: ethanol (64-17-5))
• Boiling Point: 423.4°C at 760 mmHg
• Flash Point: 188.1°C
• Appearance: /
• Density: 1.164g/cm³
• Vapor Pressure: 2.24E-07mmHg at 25°C
• Refractive Index: 1.577
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-(BENZYLOXY)-3,5-DIMETHOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(BENZYLOXY)-3,5-DIMETHOXYBENZALDEHYDE(6527-32-8)
• EPA Substance Registry System: 4-(BENZYLOXY)-3,5-DIMETHOXYBENZALDEHYDE(6527-32-8)

Safety Data

• Hazardous Substances Data: 6527-32-8(Hazardous Substances Data)

Usage

General Description

4-(Benzyloxy)-3,5-dimethoxybenzaldehyde is a chemical compound with the molecular formula C16H16O4. It is a white to pale yellow crystalline powder that is commonly used in organic synthesis and medicinal chemistry. 4-(BENZYLOXY)-3,5-DIMETHOXYBENZALDEHYDE is often used as an intermediate in the production of pharmaceuticals and agrochemicals due to its ability to undergo various chemical reactions, such as oxidation and reduction. Additionally, it has been studied for its potential therapeutic properties, including its antimicrobial and antioxidant effects. Overall, 4-(Benzyloxy)-3,5-dimethoxybenzaldehyde has a wide range of applications in the chemical and pharmaceutical industries.

InChI:InChI=1/C16H16O4/c1-18-14-8-13(10-17)9-15(19-2)16(14)20-11-12-6-4-3-5-7-12/h3-10H,11H2,1-2H3

Upstream product

• 14588-61-5 4-benzyloxy-3,5-dimethoxybenzoic acid chloride 
• 2176-18-3 4-benzyloxy-3,5-dimethoxybenzyl alcohol 
• 100-39-0 benzyl bromide 
• 134-96-3 syringic aldehyde 
• 100-44-7 benzyl chloride 
• 100-51-6 benzyl alcohol 
• 3840-31-1 (3,4,5-trimethoxyphenyl)methanol 
• 1916-07-0 3,4,5-trimethoxybenzoic acid methyl ester 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 27065-65-2 methyl 4-benzyloxy-3,5-dimethoxybenzoate 
• 14588-60-4 4-(benzyloxy)-3,5-dimethoxybenzoic acid 

Downstream Products

• 6527-33-9 4-benzyloxy-3,5-dimethoxy-β-nitrostyrene 
• 148123-49-3 2-(4-benzyloxy-3,5-dimethoxyphenyl)-2-(trimethylsilyloxy)acetonitrile 
• 136863-17-7 1-<3,5-Dimethoxyphenyl-4-(phenylmethoxy)phenyl>-2-carbethoxy-2-(2-methoxyphenoxy)ethanol 
• 136863-17-7 1-<3,5-Dimethoxyphenyl-4-(phenylmethoxy)phenyl>-2-carbethoxy-2-(2-methoxyphenoxy)ethanol 
• 76246-82-7 3-(4-benzyloxy-3,5-dimethoxyphenyl)-1-(4-benzyloxy-3-methoxyphenyl)-2-propene-1-one 
• 89307-13-1 1,3-bis(4-benzyloxy-3,5-dimethoxyphenyl)-2-propene-1-one 
• 89354-98-3 2'-hydroxy-4-benzyloxy-3,5,4',5',6'-pentamethoxychalkone 
• 141172-12-5 (Z)-1-<4-(benzyloxy)-3,5-dimethoxyphenyl>-2-(4-methoxyphenyl)ethene 
• 141172-22-7 (E)-1-<4-(benzyloxy)-3,5-dimethoxyphenyl>-2-(4-methoxyphenyl)ethene 
• 92831-75-9 <(benzyloxy-4 dimethoxy-3,5 phenyl) hydroxymethyl>-3 (benzyloxy-4 methoxy-3 benzyl)-4 dihydro-3H-furannone-2 
• 2176-18-3 4-benzyloxy-3,5-dimethoxybenzyl alcohol 
• 119030-61-4 rac-methyl (8'α)-4'-benzyloxy-7'-hydroxy-3',5'-dimethoxy-3,4-methylenedioxy-9-norlignan-9'-oates 
• 173070-70-7 (4-Benzyloxy-3,5-dimethoxy-phenyl)-(2-[1,3]dithian-2-yl-4,5-dimethoxy-phenyl)-methanol 
• 123251-25-2 4-benzyloxy-3,5-dimethoxybenzaldehyde bis(phenylthio)acetal 

Relevant articles and documents

Compound with plant growth regulating activity and preparation method thereof

The invention provides a compound with regulation and control of plant growth activity and and a preparation method of the compound. In addition, the invention relates to an application of the compound in preparation of a regulation and control plant growth medicament, and for regulating and controlling plant growth.

Sequential Cleavage of Lignin Systems by Nitrogen Monoxide and Hydrazine

The cleavage of representative lignin systems has been achieved in a metal-free two-step sequence first employing nitrogen monoxide for oxidation followed by hydrazine for reductive C?O bond scission. In combining nitrogen monoxide and lignin, the newly developed valorization strategy shows the particular feature of starting from two waste materials, and it further exploits the attractive conditions of a Wolff-Kishner reduction for C?O bond cleavage for the first time. (Figure presented.).

Iron(III)/O2-Mediated Regioselective Oxidative Cleavage of 1-Arylbutadienes to Cinnamaldehydes

A simple, efficient, and environmentally benevolent regioselective oxidative cleavage of 1-arylbutadienes to cinnamaldehydes mediated by iron(III) sulfate/O2 has been developed. The reaction offered good yields and excellent regioselectivity and showed good functional group tolerance (31 examples). The method is important, as few reports with limited substrate scope are available for such excellent oxidative cleavage of conjugated dienes.