2-(Boc-aminomethyl)benzyl Alcohol

98%

Reagent Code: #173347
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CAS Number 1333114-86-5

science Other reagents with same CAS 1333114-86-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.29 g/mol
Formula C₁₃H₁₉NO₃
badge Registry Numbers
MDL Number MFCD22418063
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in the development of protease inhibitors and peptide mimetics. Its hydroxyl and protected amine functional groups allow selective reactions, making it valuable in solid-phase and solution-phase organic synthesis. Commonly employed in the preparation of drug candidates where controlled functional group manipulation is required. Also utilized in the construction of complex heterocyclic systems through cyclization reactions. Its Boc-protected amine ensures stability during multi-step syntheses, enabling high yields and purity in final products.

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Test Parameter Specification
Appearance White to yellow powder or crystals
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,280.00

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2-(Boc-aminomethyl)benzyl Alcohol
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Used as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in the development of protease inhibitors and peptide mimetics. Its hydroxyl and protected amine functional groups allow selective reactions, making it valuable in solid-phase and solution-phase organic synthesis. Commonly employed in the preparation of drug candidates where controlled functional group manipulation is required. Also utilized in the construction of complex heterocyclic systems through cycl

Used as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in the development of protease inhibitors and peptide mimetics. Its hydroxyl and protected amine functional groups allow selective reactions, making it valuable in solid-phase and solution-phase organic synthesis. Commonly employed in the preparation of drug candidates where controlled functional group manipulation is required. Also utilized in the construction of complex heterocyclic systems through cyclization reactions. Its Boc-protected amine ensures stability during multi-step syntheses, enabling high yields and purity in final products.

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