1-(4-Bromophenyl)propan-1-amine hcl

95%

Reagent Code: #39432
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CAS Number 90485-18-0

science Other reagents with same CAS 90485-18-0

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Weight 250.5600 g/mol
Formula C₉H₁₃BrClN
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description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromophenyl group, makes it a valuable building block for creating more complex molecules, particularly in the development of drugs targeting the central nervous system. Additionally, it is employed in research settings for the synthesis of novel compounds with potential therapeutic properties, such as antidepressants or anxiolytics. The presence of the amine group allows for further chemical modifications, enabling the creation of diverse derivatives with specific biological activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,075.00

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1-(4-Bromophenyl)propan-1-amine hcl
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromophenyl group, makes it a valuable building block for creating more complex molecules, particularly in the development of drugs targeting the central nervous system. Additionally, it is employed in research settings for the synthesis of novel compounds with potential therapeutic properties, such as antid

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromophenyl group, makes it a valuable building block for creating more complex molecules, particularly in the development of drugs targeting the central nervous system. Additionally, it is employed in research settings for the synthesis of novel compounds with potential therapeutic properties, such as antidepressants or anxiolytics. The presence of the amine group allows for further chemical modifications, enabling the creation of diverse derivatives with specific biological activities.

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