Methyl 3-(hydroxymethyl)bicyclo[1.1.1]pentane-1-carboxylate

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Reagent Code: #210453
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CAS Number 180464-87-3

science Other reagents with same CAS 180464-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.18 g/mol
Formula C₈H₁₂O₃
badge Registry Numbers
MDL Number MFCD23164154
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in pharmaceutical research as a rigid building block for drug design, particularly in the development of bioisosteres to replace phenyl or other aromatic rings. Its strained bicyclic structure imparts high three-dimensionality, improving solubility and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for optimizing lead compounds, especially in CNS and protease inhibitor projects. Also utilized in the synthesis of novel analogs where steric control and reduced planarity are desired.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,600.00
inventory 250mg
10-20 days ฿3,200.00
inventory 1g
10-20 days ฿8,000.00
inventory 5g
10-20 days ฿26,660.00
inventory 10g
10-20 days ฿48,000.00

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Methyl 3-(hydroxymethyl)bicyclo[1.1.1]pentane-1-carboxylate
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Used in pharmaceutical research as a rigid building block for drug design, particularly in the development of bioisosteres to replace phenyl or other aromatic rings. Its strained bicyclic structure imparts high three-dimensionality, improving solubility and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for optimizing lead compounds, especially in CNS and protease inhibitor projects. Also utilized in the synthesis of novel analogs where steric control and reduced planari

Used in pharmaceutical research as a rigid building block for drug design, particularly in the development of bioisosteres to replace phenyl or other aromatic rings. Its strained bicyclic structure imparts high three-dimensionality, improving solubility and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for optimizing lead compounds, especially in CNS and protease inhibitor projects. Also utilized in the synthesis of novel analogs where steric control and reduced planarity are desired.

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