2-Oxaspiro[3.3]heptan-6-amine hydrochloride

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Reagent Code: #221887
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CAS Number 1523618-04-3

science Other reagents with same CAS 1523618-04-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.62 g/mol
Formula C₆H₁₂ClNO
badge Registry Numbers
MDL Number MFCD22415297
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its spirocyclic structure provides conformational rigidity, making it valuable in medicinal chemistry for enhancing metabolic stability and improving target selectivity. Commonly employed in the design of enzyme inhibitors and receptor modulators, especially within central nervous system (CNS) drug discovery. The amine functionality allows for easy derivatization, enabling rapid exploration of chemical space in structure-activity relationship (SAR) studies. Its hydrochloride salt form improves solubility and handling in aqueous reaction media.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,150.00
inventory 100mg
10-20 days ฿5,350.00
inventory 250mg
10-20 days ฿9,690.00
inventory 1g
10-20 days ฿29,150.00

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2-Oxaspiro[3.3]heptan-6-amine hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its spirocyclic structure provides conformational rigidity, making it valuable in medicinal chemistry for enhancing metabolic stability and improving target selectivity. Commonly employed in the design of enzyme inhibitors and receptor modulators, especially within central nervous system (CNS) drug discovery. The amine functionality allows for easy derivatization, en

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its spirocyclic structure provides conformational rigidity, making it valuable in medicinal chemistry for enhancing metabolic stability and improving target selectivity. Commonly employed in the design of enzyme inhibitors and receptor modulators, especially within central nervous system (CNS) drug discovery. The amine functionality allows for easy derivatization, enabling rapid exploration of chemical space in structure-activity relationship (SAR) studies. Its hydrochloride salt form improves solubility and handling in aqueous reaction media.

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