(1S,2S)-2-Methylcyclohexan-1-amine hydrochloride

98%

Reagent Code: #232506
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CAS Number 104485-19-0

science Other reagents with same CAS 104485-19-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.66164 g/mol
Formula C₇H₁₆ClN
badge Registry Numbers
MDL Number MFCD31706012
thermostat Physical Properties
Melting Point >250 °C
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring specific stereochemistry. Its rigid cyclohexyl structure and defined stereoconfiguration make it valuable for designing drugs with improved selectivity and reduced side effects. Commonly employed in asymmetric synthesis and as an intermediate in the preparation of bioactive molecules, including central nervous system agents and enzyme inhibitors. Also utilized in the creation of ligands for catalytic reactions, enhancing enantioselectivity in chemical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,270.00
inventory 100mg
10-20 days ฿14,050.00
(1S,2S)-2-Methylcyclohexan-1-amine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring specific stereochemistry. Its rigid cyclohexyl structure and defined stereoconfiguration make it valuable for designing drugs with improved selectivity and reduced side effects. Commonly employed in asymmetric synthesis and as an intermediate in the preparation of bioactive molecules, including central nervous system agents and enzyme inhibitors. Also utilized in the creati

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring specific stereochemistry. Its rigid cyclohexyl structure and defined stereoconfiguration make it valuable for designing drugs with improved selectivity and reduced side effects. Commonly employed in asymmetric synthesis and as an intermediate in the preparation of bioactive molecules, including central nervous system agents and enzyme inhibitors. Also utilized in the creation of ligands for catalytic reactions, enhancing enantioselectivity in chemical processes.

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