(4,5-dimethoxy-1,2-dihydrocyclobutabenzen-1-yl)methanamine

≥95%

Reagent Code: #180431
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CAS Number 73344-75-9

science Other reagents with same CAS 73344-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.24 g/mol
Formula C₁₁H₁₅NO₂
badge Registry Numbers
MDL Number MFCD09264101
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its strained cyclobutane ring fused to an aromatic system makes it valuable in developing novel drug candidates, particularly in central nervous system agents. The amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, or heterocycles. Also explored in materials science for designing rigid, three-dimensional molecular architectures that influence electronic or optical properties. Limited stability due to ring strain requires careful handling, but its unique geometry supports structure-activity relationship studies in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿51,750.00

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(4,5-dimethoxy-1,2-dihydrocyclobutabenzen-1-yl)methanamine
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its strained cyclobutane ring fused to an aromatic system makes it valuable in developing novel drug candidates, particularly in central nervous system agents. The amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, or heterocycles. Also explored in materials science for designing rigid, three-dimensional molecular architectures that influence electronic or optical pro

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its strained cyclobutane ring fused to an aromatic system makes it valuable in developing novel drug candidates, particularly in central nervous system agents. The amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, or heterocycles. Also explored in materials science for designing rigid, three-dimensional molecular architectures that influence electronic or optical properties. Limited stability due to ring strain requires careful handling, but its unique geometry supports structure-activity relationship studies in medicinal chemistry.

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