Trans-3-chlorocyclobutane-1-carboxylic acid

97%

Reagent Code: #238190
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CAS Number 35207-70-6

science Other reagents with same CAS 35207-70-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.56 g/mol
Formula C₅H₇ClO₂
thermostat Physical Properties
Melting Point 51-52.2 °C
Boiling Point 253.4±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.34±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules that target central nervous system disorders. Its strained cyclobutane ring and functional group arrangement make it valuable for constructing stereoselective drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and ability to mimic peptide bonds. Also utilized in the preparation of enzyme inhibitors and receptor modulators where precise spatial orientation of substituents is critical for activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,440.00
Trans-3-chlorocyclobutane-1-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules that target central nervous system disorders. Its strained cyclobutane ring and functional group arrangement make it valuable for constructing stereoselective drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and ability to mimic peptide bonds. Also utilized in the preparation

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules that target central nervous system disorders. Its strained cyclobutane ring and functional group arrangement make it valuable for constructing stereoselective drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and ability to mimic peptide bonds. Also utilized in the preparation of enzyme inhibitors and receptor modulators where precise spatial orientation of substituents is critical for activity.

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