65162-29-0

Basic information

• Product Name: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-
• CAS NO: 65162-29-0
• Molecular Formula: C9H10O4
• Molecular Weight: 182.176
• Mol File: 65162-29-0.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-(65162-29-0)
• EPA Substance Registry System: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-(65162-29-0)

Safety Data

• Hazardous Substances Data: 65162-29-0(Hazardous Substances Data)

Upstream product

• 13330-65-9 2,4-dimethoxyphenol 
• 100-97-0 hexamethylenetetramine 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 85565-93-1 2-bromo-3,5-dimethoxy-benzaldehyde 
• 829-20-9 2',4'-dimethoxyacetophenone 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 67-66-3 chloroform 

Downstream Products

• 117672-26-1 2-((Z)-2-Chloro-2-nitro-vinyl)-4,6-dimethoxy-phenol 
• 1226514-02-8 3-methoxybenzoic acid (2-hydroxy-3,5-dimethoxybenzylidene)hydrazide 
• 1226513-97-8 (4-nitrophenoxy)acetic acid (2-hydroxy-3,5-dimethoxybenzylidene)hydrazide 
• 1226513-87-6 3-(trifluoromethyl)benzoic acid (2-hydroxy-3,5-dimethoxybenzylidene)hydrazide 
• 1254062-10-6 2-(2,2-diethoxyethoxy)-3,5-dimethoxybenzaldehyde 
• 1409973-09-6 2-bromo-3,5-dimethoxy-6-hydroxy-toluene 
• 1409973-12-1 2-(3-hydroxy-3-methylbut-1-ynyl)-3,5-dimethoxy-6-hydroxytoluene 
• 1409973-06-3 benzocamphorin H 
• 65162-34-7 2-bromo-3,5-dimethoxy-6-hydroxybenzaldehyde 
• 5556-84-3 2,3,5-trimethoxy-benzaldehyde 
• 1346518-68-0 C₂₇H₂₄NO₃P 
• 1206481-92-6 3-(3',4',5'-trihydroxyphenyl)-6,8-dihydroxycoumarin 

Relevant articles and documents

Synthesis, antiepileptic effects, and structure-activity relationships of α-asarone derivatives: In vitro and in vivo neuroprotective effect of selected derivatives

In the present study, we compared the antiepileptic effects of α-asarone derivatives to explore their structure-activity relationships using the PTZ-induced seizure model. Our research revealed that electron-donating methoxy groups in the 3,4,5-position on phenyl ring increased antiepileptic potency but the placement of other groups at different positions decreased activity. Besides, in allyl moiety, the optimal activity was reached with either an allyl or a 1-butenyl group in conjugation with the benzene ring. The compounds 5 and 19 exerted better neuroprotective effects against epilepsy in vitro (cell) and in vivo (mouse) models. This study provides valuable data for further exploration and application of these compounds as potential anti-seizure medicines.

CYCLIC PEROXIDE OXIDATION OF AROMATIC COMPOUND PRODUCTION AND USE THEREOF

The present invention provides a method for converting an aromatic hydrocarbon to a phenol by providing an aromatic hydrocarbon comprising one or more aromatic C-H bonds and one or more activated C-H bonds in a solvent; adding a phthaloyl peroxide to the solvent; converting the phthaloyl peroxide to a di-radical; contacting the di-radical with the one or more aromatic C-H bonds; oxidizing selectively one of the one or more aromatic C-H bonds in preference to the one or more activated C-H bonds; adding a hydroxyl group to the one of the one or more aromatic C-H bonds to form one or more phenols; and purifying the one or more phenols.

An efficient total synthesis of Benzocamphorin H and its anti-inflammatory activity

A naturally occurring enynyl-benzenoid, Benzocamphorin H (1), from the edible fungus Taiwanofungus camphoratus (Antrodia camphorata) was characterized by the comprehensive spectral analysis. It displayed potent anti-inflammatory bioactivity and would be v