89556-60-5

Basic information

• Product Name: 1-Propanone, 1-(2,5-dimethoxyphenyl)-2-methyl-
• CAS NO: 89556-60-5
• Molecular Formula: C12H16O3
• Molecular Weight: 208.257
• Mol File: 89556-60-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1-(2,5-dimethoxyphenyl)-2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1-(2,5-dimethoxyphenyl)-2-methyl-(89556-60-5)
• EPA Substance Registry System: 1-Propanone, 1-(2,5-dimethoxyphenyl)-2-methyl-(89556-60-5)

Safety Data

• Hazardous Substances Data: 89556-60-5(Hazardous Substances Data)

Usage

Uses

Intermediate in the synthesis of various pharmaceuticals and organic compounds; key building block in the production of psychoactive drugs; potential therapeutic properties in treating mental and emotional disorders; reagent for organic synthesis in organic chemistry research; potential pharmacological effects.

Upstream product

• 79-30-1 isobutyryl chloride 
• 150-78-7 1,4-dimethoxybezene 
• 93-02-7 2,5-dimethoxybenzaldehyde 
• 155628-88-9 1-(2',5'-dimethoxyphenyl)prop-2-en-1-ol 
• 67-56-1 methanol 
• 79-31-2 isobutyric Acid 

Downstream Products

• 74587-20-5 2-pivaloyl-1,4-bezoquinone 
• 35459-97-3 2',5'-dihydroxypivalophenone 
• 89556-70-7 1-<2,5-dimethoxy-4-(2-methylpropyl)phenyl>-2-aminopropane 
• 89556-63-8 1-<2,5-dimethoxy-4-(2-methylpropyl)phenyl>-2-nitropropene 
• 89556-62-7 2,5-dimethoxy-4-(2-methylpropyl)benzaldehyde 
• 35205-30-2 1-(2,5-dimethoxyphenyl)-2-methylpropene 
• 89556-61-6 1-(2,5-dimethoxyphenyl)-2-methylpropane 
• 73566-49-1 isobutyryl-1,4-benzoquinone 
• 39868-14-9 2,5-Dimethoxyphenyl tert-butyl ketone 
• 112450-27-8 1-(2,5-dihydroxy-phenyl)-2-methyl-propan-1-one 
• 26172-15-6 1-(2,5-dimethoxyphenyl)-2-methyl-1-propanol 
• 109497-49-6 5-(2,5-dimethoxy-phenyl)-4-methyl-[1,2]dithiol-3-thione 

Relevant articles and documents

Palladium-Catalyzed Synthesis of α-Methyl Ketones from Allylic Alcohols and Methanol

One-pot synthesis of α-methyl ketones starting from 1,3-diaryl propenols or 1-aryl propenols and methanol as a C1 source is demonstrated. This one-pot isomerization-methylation is catalyzed by commercially available Pd(OAc)2 with H2O as the only by-product. Mechanistic studies and deuterium labelling experiments indicate the involvement of isomerization of allyl alcohol followed by methylation through a hydrogen-borrowing pathway in these isomerization-methylation reactions.

Substituent Branching in Phenethylamine-Type Hallucinogens: A Comparison of 1--2-aminopropane and 1--2-aminopropane

Two novel hallucinogen analogues related to 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM, STP) were synthesized and evaluated in the two-lever drug discrimination paradigm by using 0.08 mg/kg of LSD at the training drug stimulus.The two compounds