Benzyl (5-hydroxypentyl)carbamate

96%

Reagent Code: #148215
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CAS Number 87905-98-4

science Other reagents with same CAS 87905-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.30 g/mol
Formula C₁₃H₁₉NO₃
badge Registry Numbers
MDL Number MFCD01863135
thermostat Physical Properties
Boiling Point 408.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure allows for selective protection of amine groups, making it valuable in peptide synthesis and drug development. The hydroxyl group enables further functionalization, facilitating the creation of prodrugs or modified molecules with improved solubility and bioavailability. It is also employed in the design of enzyme inhibitors and receptor ligands due to its ability to mimic natural substrates.

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Test Parameter Specification
Appearance White to Pale Grey Low-Melting Solid
Purity (%) 95.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,690.00
inventory 1g
10-20 days ฿3,710.00
inventory 5g
10-20 days ฿18,340.00

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Benzyl (5-hydroxypentyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure allows for selective protection of amine groups, making it valuable in peptide synthesis and drug development. The hydroxyl group enables further functionalization, facilitating the creation of prodrugs or modified molecules with improved solubility and bioavailability. It is also employed in the design of enzyme inhibitors and receptor ligands due to its abili

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure allows for selective protection of amine groups, making it valuable in peptide synthesis and drug development. The hydroxyl group enables further functionalization, facilitating the creation of prodrugs or modified molecules with improved solubility and bioavailability. It is also employed in the design of enzyme inhibitors and receptor ligands due to its ability to mimic natural substrates.

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