Ethyl 2-(cyclopentylamino)benzoate

95%

Reagent Code: #183726
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CAS Number 1094227-86-7

science Other reagents with same CAS 1094227-86-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.31 g/mol
Formula C₁₄H₁₉NO₂
badge Registry Numbers
MDL Number MFCD11179069
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for functionalization in the development of central nervous system agents, particularly in the design of analogs with potential anxiolytic or sedative properties. The ester and amine groups enable coupling reactions and ring formation, making it valuable in medicinal chemistry for constructing heterocyclic systems. It may also find use in the synthesis of local anesthetics or anti-inflammatory agents due to its benzoate backbone and modifiable amine moiety.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿11,660.00
inventory 1g
10-20 days ฿32,420.00

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Ethyl 2-(cyclopentylamino)benzoate
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for functionalization in the development of central nervous system agents, particularly in the design of analogs with potential anxiolytic or sedative properties. The ester and amine groups enable coupling reactions and ring formation, making it valuable in medicinal chemistry for constructing heterocyclic systems. It may also find use in the syn

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for functionalization in the development of central nervous system agents, particularly in the design of analogs with potential anxiolytic or sedative properties. The ester and amine groups enable coupling reactions and ring formation, making it valuable in medicinal chemistry for constructing heterocyclic systems. It may also find use in the synthesis of local anesthetics or anti-inflammatory agents due to its benzoate backbone and modifiable amine moiety.

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