trans-2-(3-methoxyphenyl)cyclopropane-1-carboxylic acid

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Reagent Code: #241786
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CAS Number 34919-31-8

science Other reagents with same CAS 34919-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.21 g/mol
Formula C₁₁H₁₂O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its rigid cyclopropane structure and functional groups make it valuable for designing enzyme inhibitors and receptor modulators. Commonly employed in the development of analgesics and anticonvulsant drugs due to its ability to influence neuronal ion channel activity. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,950.00
inventory 500mg
10-20 days ฿8,550.00
inventory 1g
10-20 days ฿14,220.00
inventory 5g
10-20 days ฿59,400.00
inventory 100mg
10-20 days ฿1,728.00

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trans-2-(3-methoxyphenyl)cyclopropane-1-carboxylic acid
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its rigid cyclopropane structure and functional groups make it valuable for designing enzyme inhibitors and receptor modulators. Commonly employed in the development of analgesics and anticonvulsant drugs due to its ability to influence neuronal ion channel activity. Also utilized in asymmetric synthesis to introduce stereochemical control in com

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its rigid cyclopropane structure and functional groups make it valuable for designing enzyme inhibitors and receptor modulators. Commonly employed in the development of analgesics and anticonvulsant drugs due to its ability to influence neuronal ion channel activity. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.

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