(1r,4r)-4-(aminomethyl)-1-methylcyclohexanol 4-methylbenzenesulfonate

97%

Reagent Code: #229112
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CAS Number 1630101-52-8

science Other reagents with same CAS 1630101-52-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.43 g/mol
Formula C₁₅H₂₅NO₄S
badge Registry Numbers
MDL Number MFCD28334268
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of functional groups that can be modified for enhanced binding and selectivity. Commonly employed in the preparation of analgesics and muscle relaxants, where the aminomethyl and hydroxyl groups contribute to receptor interaction and solubility. The tosylate form improves crystallinity and stability, making it suitable for purification and formulation processes in drug manufacturing.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20,030.00
(1r,4r)-4-(aminomethyl)-1-methylcyclohexanol 4-methylbenzenesulfonate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of functional groups that can be modified for enhanced binding and selectivity. Commonly employed in the preparation of analgesics and muscle relaxants, where the aminomethyl and hydroxyl groups contribute to receptor interaction and solubility. The tosylate form improves crystallinity and sta

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of functional groups that can be modified for enhanced binding and selectivity. Commonly employed in the preparation of analgesics and muscle relaxants, where the aminomethyl and hydroxyl groups contribute to receptor interaction and solubility. The tosylate form improves crystallinity and stability, making it suitable for purification and formulation processes in drug manufacturing.

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