41395-10-2

Basic information

• Product Name: Benzene, 1,3-dimethoxy-5-propyl-
• CAS NO: 41395-10-2
• Molecular Formula: C11H16O2
• Molecular Weight: 180.247
• Mol File: 41395-10-2.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: Benzene, 1,3-dimethoxy-5-propyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,3-dimethoxy-5-propyl-(41395-10-2)
• EPA Substance Registry System: Benzene, 1,3-dimethoxy-5-propyl-(41395-10-2)

Safety Data

• Hazardous Substances Data: 41395-10-2(Hazardous Substances Data)

Upstream product

• 41497-31-8 3,5-dimethoxyphenyl ethyl ketone 
• 487-11-6 elemicin 
• 41564-88-9 1-(3',4',5'-trimethoxyphenyl)propane 
• 502924-54-1 3-(3,5-dimethoxy-phenyl)-2-methyl-3-oxo-propionic acid ethyl ester 
• 55136-70-4 3-methoxy-5-propylphenol 
• 74-88-4 methyl iodide 
• 52189-64-7 2,4-dimethoxy-6-propylbenzoic acid 
• 203912-55-4 1-(3,5-dimethoxy-phenyl)-propan-1-ol 
• 52189-63-6 3,5-dimethoxyfluorobenzene 
• 106-94-5 propyl bromide 
• 7051-16-3 1-chloro-3,5-dimethoxybenzene 
• 107-08-4 1-iodo-propane 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 500-49-2 5-propyl-1,3-benzenediol 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 83036-49-1 1,3-Dimethoxy-2-(3-methyl-but-2-enyl)-5-propyl-benzene 
• 83036-50-4 1,5-Dimethoxy-2-(3-methyl-but-2-enyl)-3-propyl-benzene 
• 83036-51-5 2-((E)-3,7-Dimethyl-octa-2,6-dienyl)-1,3-dimethoxy-5-propyl-benzene 
• 83036-52-6 2-((E)-3,7-Dimethyl-octa-2,6-dienyl)-1,5-dimethoxy-3-propyl-benzene 
• 55136-70-4 3-methoxy-5-propylphenol 
• 104307-42-8 2-iodo-1,5-dimethoxy-3-propylbenzene 
• 70680-17-0 2-Pentyl-5-propylresorcin 
• 39341-78-1 2-hexyl-5-propyl-1,3-benzenediol 
• 69505-82-4 2-Heptyl-5-propylresorcin 
• 39503-21-4 2,6-Dimethoxy-4-propylbenzaldehyd 
• 39503-19-0 2,4-dimethoxy-6-propylbenzaldehyde 
• 203912-56-5 2,6-dimethoxy-4-n-propylphenylacetaldehyde 

Relevant articles and documents

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

The invention belongs to the technical field of medicines, and discloses an aromatic compound hydrogenation and hydrodeoxygenation method under mild conditions and application of the method in hydrogenation and hydrodeoxygenation reactions of the aromatic compounds and related mixtures. Specifically, the method comprises the following steps: contacting the aromatic compound or a mixture containing the aromatic compound with a catalyst and hydrogen with proper pressure in a solvent under a proper temperature condition, and reacting the hydrogen, the solvent and the aromatic compound under the action of the catalyst to obtain a corresponding hydrogenation product or/and a hydrodeoxygenation product without an oxygen-containing substituent group. The invention also discloses specific implementation conditions of the method and an aromatic compound structure type applicable to the method. The hydrogenation and hydrodeoxygenation reaction method used in the invention has the advantages of mild reaction conditions, high hydrodeoxygenation efficiency, wide substrate applicability, convenient post-treatment, and good laboratory and industrial application prospects.

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