N-(4-Chloro-2,5-dimethoxyphenyl)acetamide

≥95%

Reagent Code: #215158
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CAS Number 6938-75-6

science Other reagents with same CAS 6938-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.6602 g/mol
Formula C₁₀H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD00048193
thermostat Physical Properties
Melting Point 116-117 °C
Boiling Point 371.3±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.258±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of psychoactive substances, particularly in the production of certain hallucinogenic phenethylamines. It serves as a key precursor in clandestine chemistry for compounds like 2C-C, due to the presence of the dimethoxy and chloro substituents that are characteristic of this class of psychedelics. Its acetylated amine group stabilizes the molecule during synthesis, allowing for further chemical modifications before deprotection and final product formation. Limited to research and forensic interest, with no approved pharmaceutical or industrial applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿16,000.00
250mg
10-20 days ฿32,000.00
1g
10-20 days ฿96,000.00
N-(4-Chloro-2,5-dimethoxyphenyl)acetamide
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Used primarily as an intermediate in the synthesis of psychoactive substances, particularly in the production of certain hallucinogenic phenethylamines. It serves as a key precursor in clandestine chemistry for compounds like 2C-C, due to the presence of the dimethoxy and chloro substituents that are characteristic of this class of psychedelics. Its acetylated amine group stabilizes the molecule during synthesis, allowing for further chemical modifications before deprotection and final product formation.

Used primarily as an intermediate in the synthesis of psychoactive substances, particularly in the production of certain hallucinogenic phenethylamines. It serves as a key precursor in clandestine chemistry for compounds like 2C-C, due to the presence of the dimethoxy and chloro substituents that are characteristic of this class of psychedelics. Its acetylated amine group stabilizes the molecule during synthesis, allowing for further chemical modifications before deprotection and final product formation. Limited to research and forensic interest, with no approved pharmaceutical or industrial applications.

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