Benzyl (3-hydroxycyclopentyl)carbamate

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Reagent Code: #145713
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CAS Number 939426-84-3

science Other reagents with same CAS 939426-84-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.28 g/mol
Formula C₁₃H₁₇NO₃
badge Registry Numbers
MDL Number MFCD11848126
thermostat Physical Properties
Boiling Point 415.1±44.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for compounds with potential anxiolytic or sedative properties due to its structural similarity to bioactive cyclopentyl derivatives. Also employed in medicinal chemistry research to explore structure-activity relationships in carbamate-based molecules. Its hydroxyl and carbamate functional groups allow for further chemical modifications, making it valuable in creating compound libraries for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿690.00
inventory 100mg
10-20 days ฿1,670.00
inventory 250mg
10-20 days ฿2,650.00
inventory 1g
10-20 days ฿6,780.00
inventory 5g
10-20 days ฿23,750.00

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Benzyl (3-hydroxycyclopentyl)carbamate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for compounds with potential anxiolytic or sedative properties due to its structural similarity to bioactive cyclopentyl derivatives. Also employed in medicinal chemistry research to explore structure-activity relationships in carbamate-based molecules. Its hydroxyl and carbamate functional groups allow for further chemical modifications, making it v

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for compounds with potential anxiolytic or sedative properties due to its structural similarity to bioactive cyclopentyl derivatives. Also employed in medicinal chemistry research to explore structure-activity relationships in carbamate-based molecules. Its hydroxyl and carbamate functional groups allow for further chemical modifications, making it valuable in creating compound libraries for drug discovery.

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