41317-93-5

Basic information

• Product Name: Benzenemethanol, 2,4,5-trimethoxy-a-methyl-
• CAS NO: 41317-93-5
• Molecular Formula: C11H16O4
• Molecular Weight: 212.246
• Mol File: 41317-93-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2,4,5-trimethoxy-a-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2,4,5-trimethoxy-a-methyl-(41317-93-5)
• EPA Substance Registry System: Benzenemethanol, 2,4,5-trimethoxy-a-methyl-(41317-93-5)

Safety Data

• Hazardous Substances Data: 41317-93-5(Hazardous Substances Data)

Upstream product

• 1818-28-6 2',4',5'-trimethoxyacetophenone 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 74-83-9 methyl bromide 
• 4460-86-0 asaraldehyde 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 1818-28-6 2',4',5'-trimethoxyacetophenone 
• 17598-03-7 5-ethenyl-1,2,4-trimethoxybenzene 

Relevant articles and documents

Compound for treating or preventing hepatopathy (by machine translation)

The invention discloses a compound, an optical isomer or a pharmaceutically acceptable salt, an optical isomer or a pharmaceutically acceptable salt thereof for treating or preventing hepatopathy, and the compound, optical isomer or pharmaceutically acceptable salt thereof can be applied to the preparation of a medicine for treating or preventing liver diseases. (by machine translation)

An effective system to synthesize hypolipidemic active α-asarone and related methoxylated (E)-arylalkenes

Methoxylated (E)-arylalkenes (1a-1k) were prepared in two steps by an improved Grignard reaction comprising the reverse addition of alkylmagnesium bromide to benzaldehydes (2a-2k) in anhydrous ether and toluene into arylalkanols (3a-3k) in high yield, followed by dehydration with silica gel under microwave irradiation for 3-12 min, depending upon the substituents attached to the aromatic ring to afford hypolipidemic active α-asarone (1a) and related methoxylated (E)-arylalkenes (1b-1k).