2801-68-5

Basic information

• Product Name: 1-(2 5-DIMETHOXYPHENYL)-2-AMINOPROPANE&
• Synonyms: (+-)-2,5-dimethoxyamphetamine;2-(2,5-Dimethoxyphenyl)-1-methylethylamine;2,5-Dimethoxy-α-methylbenzeneethanamine;C-1739;α-Methyl-2,5-dimethoxybenzeneethanamine;1-(2,5-dimethoxyphenyl)propan-2-amine;2,5-Dimethoxyamphetamine (exempt preparation);1-(2,5-dimethoxyphenyl)-2-aminopropane
• CAS NO: 2801-68-5
• Molecular Formula: C₁₁H₁₇NO₂
• Molecular Weight: 195.25818
• EINECS: 220-540-2
• Product Categories: 2,5-DMA
• Mol File: 2801-68-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 350.94°C (rough estimate)
• Appearance: /
• Density: 1.1240 (rough estimate)
• Refractive Index: 1.5718 (estimate)
• PKA: 9.76±0.10(Predicted)
• CAS DataBase Reference: 1-(2 5-DIMETHOXYPHENYL)-2-AMINOPROPANE&(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2 5-DIMETHOXYPHENYL)-2-AMINOPROPANE&(2801-68-5)
• EPA Substance Registry System: 1-(2 5-DIMETHOXYPHENYL)-2-AMINOPROPANE&(2801-68-5)

Safety Data

• Hazard Codes: T
• Statements: 23/24/25
• Safety Statements: 36/37/39-45
• RIDADR: UN 2811 6.1/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 2801-68-5(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Oil

Uses

Amphetamine derivative. Hallucinogenic.

Upstream product

• 134040-27-0 2,5-dimethoxy-β-methyl-β-nitrostyrene 
• 210104-56-6 3-(2,5-dimethoxy-phenyl)-2-methyl-propionic acid 
• 262603-21-4 2-(β-p-nitrobenzenesulfonyloxypropyl)-1,4-dimethoxybenzene 
• 262603-22-5 2-(β-benzenesulfonyloxypropyl)-1,4-dimethoxybenzene 
• 77404-73-0 2-(β-tosyloxypropyl)-1,4-dimethoxybenzene 
• 79-24-3 Nitroethane 
• 93-02-7 2,5-dimethoxybenzaldehyde 
• 18790-57-3 (E)-1,4-dimethoxy-2-(2-nitroprop-1-en-1-yl) benzene 
• 858214-52-5 3-(2,5-dimethoxy-phenyl)-2-methyl-propionic acid amide 
• 854838-13-4 (2,5-dimethoxy-benzyl)-methyl-malonic acid 
• 150-78-7 1,4-dimethoxybezene 
• 40180-96-9 2-(β-hydroxypropyl)-1,4-dimethoxybenzene 

Downstream Products

• 67707-78-2 N,N-dimethyl-2-(2,5-dimethoxyphenyl)isopropylamine 
• 54687-43-3 [2-(2,5-dimethoxy-phenyl)-1-methyl-ethyl]-methyl-amine 
• 64584-34-5 4-iodo-2,5-dimethoxyphenylisopropylamine 
• 67460-68-8 1-(2,5-dimethoxy-4-nitrophenyl) propan-2-amine 
• 99632-44-7 N-propionyl-1-(2,5-dimethoxyphenyl)-2-aminopropane 
• 79315-43-8 (+/-)-N-[2-(2,5-dimethoxyphenyl)-1-methylethyl]-2,2,2-trifluoroacetamide 
• 58993-81-0 (-)-DMA 
• 58993-80-9 (S)-2-(2,5-dimethoxy-phenyl)-1-methyl-ethylamine 
• 125903-73-3 1-(4-benzyl-2,5-dimethoxyphenyl)-2-aminopropane 
• 125903-72-2 1-[2,5-dimethoxy-4-(3-phenylpropyl)phenyl]-2-aminopropane 
• 125903-71-1 1-(2,5-dimethoxy-4-octylphenyl)-2-aminopropane 
• 23092-91-3 1-(2,5-dimethoxy-4-hexylphenyl)-2-aminopropane 
• 125926-18-3 1-(2,5-dimethoxy-4-propionylphenyl)-2-aminopropane 
• 125926-55-8 N-(trifluoroacetyl)-1-(2,5-dimethoxy-4-hydrocinnamoylphenyl)-2-aminopropane 

Relevant articles and documents

Immunoassay for Phenethylamines of the 2C and DO Sub-Families

Immunoassay methods and their requisite components for the detection and determination of phenethylamines of the 2C and DO sub-families are described.

New route to 2-(β-aminopropyl)-1,4-dimethoxybenzene

A new synthetic route was proposed and an original procedure developed for preparing 2-(β-aminopropyl)-1,4-dimethoxybenzene, which is an important intermediate in synthesis of a blue developing dye for color instant-picture process of the Polaroid type.

The synthesis of some analogs of the hallucinogen 1 (2,5 dimethoxy 4 methylphenyl) 2 aminopropane (DOM)

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