4-(2-(methoxycarbonyl)cyclopropyl)benzoic acid

≥95%

Reagent Code: #213399
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CAS Number 1057107-39-7

science Other reagents with same CAS 1057107-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.22 g/mol
Formula C₁₂H₁₂O₄
badge Registry Numbers
MDL Number MFCD22393665
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of antidiabetic drugs, particularly in the production of SGLT2 inhibitors like canagliflozin. Its structure allows for the formation of cyclopropane-containing motifs that are critical for biological activity in this class of pharmaceuticals. The carboxylic and ester functional groups enable further chemical modifications, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in coupling reactions to attach aromatic and sugar moieties during drug development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿29,740.00
4-(2-(methoxycarbonyl)cyclopropyl)benzoic acid
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Used as a key intermediate in the synthesis of antidiabetic drugs, particularly in the production of SGLT2 inhibitors like canagliflozin. Its structure allows for the formation of cyclopropane-containing motifs that are critical for biological activity in this class of pharmaceuticals. The carboxylic and ester functional groups enable further chemical modifications, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in coupling reactions to attach aromatic and sug

Used as a key intermediate in the synthesis of antidiabetic drugs, particularly in the production of SGLT2 inhibitors like canagliflozin. Its structure allows for the formation of cyclopropane-containing motifs that are critical for biological activity in this class of pharmaceuticals. The carboxylic and ester functional groups enable further chemical modifications, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in coupling reactions to attach aromatic and sugar moieties during drug development.

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