(1R,2R)-2-Methoxycyclobutanamine hydrochloride

98%

Reagent Code: #229347
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CAS Number 1820576-22-4

science Other reagents with same CAS 1820576-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.61 g/mol
Formula C₅H₁₂ClNO
badge Registry Numbers
MDL Number MFCD31616349
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a chiral building block for pharmaceuticals. Its rigid cyclobutane structure and defined stereochemistry make it valuable for developing bioactive molecules, particularly in the design of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational constraints. Also utilized in asymmetric synthesis as a chiral amine auxiliary or catalyst precursor. The hydrochloride salt form enhances stability and solubility in aqueous reaction systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,600.00
inventory 500mg
10-20 days ฿24,000.00
inventory 1g
10-20 days ฿33,600.00
(1R,2R)-2-Methoxycyclobutanamine hydrochloride
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Used in organic synthesis as a chiral building block for pharmaceuticals. Its rigid cyclobutane structure and defined stereochemistry make it valuable for developing bioactive molecules, particularly in the design of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational constraints. Also utilized in asymmetric synthesis as a chiral amine auxiliary or catalyst precursor. The hydrochloride salt form enhan

Used in organic synthesis as a chiral building block for pharmaceuticals. Its rigid cyclobutane structure and defined stereochemistry make it valuable for developing bioactive molecules, particularly in the design of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational constraints. Also utilized in asymmetric synthesis as a chiral amine auxiliary or catalyst precursor. The hydrochloride salt form enhances stability and solubility in aqueous reaction systems.

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