1-Cyclobutylethan-1-amine hydrochloride

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Reagent Code: #163327
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CAS Number 904733-73-9

science Other reagents with same CAS 904733-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.64 g/mol
Formula C₆H₁₄ClN
badge Registry Numbers
MDL Number MFCD19690555
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where cyclobutyl groups contribute to metabolic stability and improved binding affinity. Its amine functionality allows for coupling reactions in medicinal chemistry, making it valuable in creating novel drug candidates. Commonly employed in research settings for structure-activity relationship (SAR) studies due to the constrained cyclobutane ring, which influences conformation and bioavailability. Also utilized in the preparation of catalysts and chiral ligands for asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,480.00
inventory 250mg
10-20 days ฿7,690.00
inventory 1g
10-20 days ฿26,640.00

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1-Cyclobutylethan-1-amine hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where cyclobutyl groups contribute to metabolic stability and improved binding affinity. Its amine functionality allows for coupling reactions in medicinal chemistry, making it valuable in creating novel drug candidates. Commonly employed in research settings for structure-activity relationship (SAR) studies due to the constrained cyclobutane ring, which influences conf

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where cyclobutyl groups contribute to metabolic stability and improved binding affinity. Its amine functionality allows for coupling reactions in medicinal chemistry, making it valuable in creating novel drug candidates. Commonly employed in research settings for structure-activity relationship (SAR) studies due to the constrained cyclobutane ring, which influences conformation and bioavailability. Also utilized in the preparation of catalysts and chiral ligands for asymmetric synthesis.

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