6,6-Difluorospiro[3.3]heptan-2-ylmethanaminehydrochloride

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Reagent Code: #179780
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CAS Number 1638765-23-7

science Other reagents with same CAS 1638765-23-7

blur_circular Chemical Specifications

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Weight 197.65 g/mol
Formula C₈H₁₄ClF₂N
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MDL Number MFCD23106458
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its spirocyclic structure with fluorination enhances metabolic stability and membrane permeability, making it valuable in drug design for improving pharmacokinetic properties. Commonly employed in the development of novel neuroactive agents, including potential anticonvulsants and anxiolytics. The amine functionality allows for easy derivatization, facilitating the creation of compound libraries for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,020.00
inventory 250mg
10-20 days ฿45,660.00

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6,6-Difluorospiro[3.3]heptan-2-ylmethanaminehydrochloride
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its spirocyclic structure with fluorination enhances metabolic stability and membrane permeability, making it valuable in drug design for improving pharmacokinetic properties. Commonly employed in the development of novel neuroactive agents, including potential anticonvulsants and anxiolytics. The amine functionality allows for easy derivatization, faci

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its spirocyclic structure with fluorination enhances metabolic stability and membrane permeability, making it valuable in drug design for improving pharmacokinetic properties. Commonly employed in the development of novel neuroactive agents, including potential anticonvulsants and anxiolytics. The amine functionality allows for easy derivatization, facilitating the creation of compound libraries for structure-activity relationship studies.

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