3-(Difluoromethyl)bicyclo[1.1.1]pentan-1-amine hydrochloride

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Reagent Code: #131339
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CAS Number 2108549-79-5

science Other reagents with same CAS 2108549-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.6 g/mol
Formula C₆H₁₀ClF₂N
badge Registry Numbers
MDL Number MFCD29767886
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in pharmaceutical development as a bioisostere for phenyl or other aromatic groups, enhancing metabolic stability and improving pharmacokinetic properties. The 3-difluoromethyl substituent provides additional electronic modulation and resistance to enzymatic degradation. Its rigid bicyclo[1.1.1]pentane structure helps modulate lipophilicity and solubility, making it valuable in medicinal chemistry for central nervous system drugs and other therapeutic agents. Commonly incorporated into drug candidates to replace metabolically labile groups, reducing off-target effects and increasing in vivo half-life. Also applied in agrochemicals for optimizing molecular geometry and enhancing target binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,320.00
inventory 250mg
10-20 days ฿34,050.00

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3-(Difluoromethyl)bicyclo[1.1.1]pentan-1-amine hydrochloride
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Used in pharmaceutical development as a bioisostere for phenyl or other aromatic groups, enhancing metabolic stability and improving pharmacokinetic properties. The 3-difluoromethyl substituent provides additional electronic modulation and resistance to enzymatic degradation. Its rigid bicyclo[1.1.1]pentane structure helps modulate lipophilicity and solubility, making it valuable in medicinal chemistry for central nervous system drugs and other therapeutic agents. Commonly incorporated into drug candidat

Used in pharmaceutical development as a bioisostere for phenyl or other aromatic groups, enhancing metabolic stability and improving pharmacokinetic properties. The 3-difluoromethyl substituent provides additional electronic modulation and resistance to enzymatic degradation. Its rigid bicyclo[1.1.1]pentane structure helps modulate lipophilicity and solubility, making it valuable in medicinal chemistry for central nervous system drugs and other therapeutic agents. Commonly incorporated into drug candidates to replace metabolically labile groups, reducing off-target effects and increasing in vivo half-life. Also applied in agrochemicals for optimizing molecular geometry and enhancing target binding affinity.

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