[1-(2,6-Dichlorophenyl)cyclobutyl]methanamine

98%

Reagent Code: #178754
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CAS Number 760157-03-7

science Other reagents with same CAS 760157-03-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.13 g/mol
Formula C₁₁H₁₃Cl₂N
badge Registry Numbers
MDL Number MFCD11188917
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structural features make it valuable in the preparation of analogs targeting neurological disorders such as depression, anxiety, and neuropathic pain. The amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, or secondary amines to fine-tune pharmacological properties. It is also employed in medicinal chemistry research to explore structure-activity relationships (SAR) in novel drug candidates. Due to the steric and electronic influence of the dichlorophenyl and cyclobutyl groups, it contributes to metabolic stability and target selectivity in active molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿32,110.00
inventory 50mg
10-20 days ฿9,090.00

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[1-(2,6-Dichlorophenyl)cyclobutyl]methanamine
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Used primarily as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structural features make it valuable in the preparation of analogs targeting neurological disorders such as depression, anxiety, and neuropathic pain. The amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, or secondary amines to fine-tune pharmacological properties. It is also employed in medicinal chemistry research to explore structure-activity relationships (SAR) in novel drug candidates. Due to the steric and electronic influence of the dichlorophenyl and cyclobutyl groups, it contributes to metabolic stability and target selectivity in active molecules.
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