cis-3-Methoxycyclobutanecarboxylic acid

97%

Reagent Code: #202949
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CAS Number 552849-35-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.14 g/mol
Formula C₆H₁₀O₃
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MDL Number MFCD22396943
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and enzyme inhibitors. Its strained cyclobutane ring and functional group positioning make it valuable for modifying metabolic stability and binding affinity in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and stereochemical control. Also utilized in the preparation of bioactive molecules where a small, polar ring system is needed to enhance solubility and reduce lipophilicity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿38,000.00
cis-3-Methoxycyclobutanecarboxylic acid
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Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and enzyme inhibitors. Its strained cyclobutane ring and functional group positioning make it valuable for modifying metabolic stability and binding affinity in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and stereochemical control. Also utilized in the preparation

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and enzyme inhibitors. Its strained cyclobutane ring and functional group positioning make it valuable for modifying metabolic stability and binding affinity in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and stereochemical control. Also utilized in the preparation of bioactive molecules where a small, polar ring system is needed to enhance solubility and reduce lipophilicity.

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