tert-Butyl 4-cyanobenzylcarbamate

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Reagent Code: #148258
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CAS Number 66389-80-8

science Other reagents with same CAS 66389-80-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.28 g/mol
Formula C₁₃H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD08436197
thermostat Physical Properties
Boiling Point 392.9°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.1 g/cm3
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protection of amine functionalities is required. The tert-butyloxycarbonyl (Boc) group provides stability during multi-step reactions and can be selectively removed under mild acidic conditions, making it valuable in peptide and heterocyclic chemistry. The cyanobenzyl moiety can serve as a precursor for further functionalization, such as conversion to tetrazoles or carboxylic acids, useful in drug design for bioisosteric replacements or metabolic stability enhancement. Commonly employed in research settings for constructing complex molecules in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿840.00
inventory 5g
10-20 days ฿3,480.00
inventory 10g
10-20 days ฿6,600.00
inventory 25g
10-20 days ฿16,330.00

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tert-Butyl 4-cyanobenzylcarbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protection of amine functionalities is required. The tert-butyloxycarbonyl (Boc) group provides stability during multi-step reactions and can be selectively removed under mild acidic conditions, making it valuable in peptide and heterocyclic chemistry. The cyanobenzyl moiety can serve as a precursor for further functionalization, such as conversion to tet

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protection of amine functionalities is required. The tert-butyloxycarbonyl (Boc) group provides stability during multi-step reactions and can be selectively removed under mild acidic conditions, making it valuable in peptide and heterocyclic chemistry. The cyanobenzyl moiety can serve as a precursor for further functionalization, such as conversion to tetrazoles or carboxylic acids, useful in drug design for bioisosteric replacements or metabolic stability enhancement. Commonly employed in research settings for constructing complex molecules in medicinal chemistry.

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