Benzyl (2,4-difluoro-3-formylphenyl)carbamate

97%

Reagent Code: #148568
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CAS Number 918524-07-9

science Other reagents with same CAS 918524-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.25 g/mol
Formula C₁₅H₁₁F₂NO₃
badge Registry Numbers
MDL Number MFCD21648244
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde group allows for further functionalization via reactions such as reductive amination or condensation, enabling the construction of complex drug molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide bonds and enhance metabolic stability. Also utilized in the preparation of protease inhibitors and anti-inflammatory agents.

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Test Parameter Specification
Appearance White to yellow powder or crystals
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿500.50
inventory 250mg
10-20 days ฿1,116.50

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Benzyl (2,4-difluoro-3-formylphenyl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde group allows for further functionalization via reactions such as reductive amination or condensation, enabling the construction of complex drug molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide bonds and enhance metabolic stability. Also utilized in the preparati

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde group allows for further functionalization via reactions such as reductive amination or condensation, enabling the construction of complex drug molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide bonds and enhance metabolic stability. Also utilized in the preparation of protease inhibitors and anti-inflammatory agents.

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