203579-18-4

Basic information

• Product Name: 4-ethyl-3,5-dimethoxybenzyl alcohol
• Synonyms: 4-ethyl-3,5-dimethoxybenzyl alcohol
• CAS NO: 203579-18-4
• Molecular Weight: 196.246
• Mol File: 203579-18-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-ethyl-3,5-dimethoxybenzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ethyl-3,5-dimethoxybenzyl alcohol(203579-18-4)
• EPA Substance Registry System: 4-ethyl-3,5-dimethoxybenzyl alcohol(203579-18-4)

Safety Data

• Hazardous Substances Data: 203579-18-4(Hazardous Substances Data)

Upstream product

• 78025-99-7 3,5-dimethoxy-4-ethylbenzaldehyde 

Downstream Products

• 144538-13-6 (+)-O-methylasparvenone 
• 203579-28-6 6-Ethyl-5-methoxy-7-(1-phenyl-1H-tetrazol-5-yloxy)-3H-isobenzofuran-1-one 
• 56495-98-8 O-methylasparvenone 
• 136458-96-3 (+/-)-O-methylasparvenone 
• 204650-27-1 cis-7-ethyl-6-hydroxy-8-methoxy-2-methyl-1,2,3,3a,4,9b-hexahydro-5H-benzo[e]isoindol-5-one 
• 204650-26-0 [4-(4-Ethyl-3,5-dimethoxy-phenyl)-1-methyl-2-oxo-pyrrolidin-3-yl]-acetic acid tert-butyl ester 
• 204650-05-5 4-Cyano-4-(4-ethyl-3,5-dimethoxy-phenyl)-butyric acid methyl ester 
• 204650-06-6 3-Cyano-3-(4-ethyl-3,5-dimethoxy-phenyl)-propionic acid ethyl ester 
• 204650-25-9 4-(4-ethyl-3,5-dimethoxy-phenyl)-1-methyl-pyrrolidin-2-one 
• 1071160-15-0 4-Amino-3-(4-ethyl-3,5-dimethoxy-phenyl)-butyric acid 
• 204650-07-7 5-Amino-4-(4-ethyl-3,5-dimethoxy-phenyl)-pentanoic acid 
• 204650-24-8 4-(4-ethyl-3,5-dimethoxy-phenyl)-pyrrolidin-2-one 
• 204650-04-4 (4-Ethyl-3,5-dimethoxy-phenyl)-acetonitrile 
• 204650-48-6 5-Chloromethyl-2-ethyl-1,3-dimethoxy-benzene 

Relevant articles and documents

O-Methylasparvenone, a Nitrogen-free Serotonin Antagonist

O-Methylasparvenone (1) and asparvenone (2) were isolated from an Aspergillus parvulus Smith broth in a microbial screening for 5-HT2C ligands and found to be 5-HT2C antagonists.They represent the first nitrogen-free serotonin ligands.The absolute configuration of 1 was determined to be S by X-ray analysis of the corresponding Mosher-ester.A short and efficient synthesis of rac-1 was developed.This protocol was applied to the synthesis of derivatives of 1 and a structure-affinity relationship was established.