tert-Butyl (1-chloro-2-oxo-7,10,13-trioxa-3-azahexadecan-16-yl)carbamate

≥95%

Reagent Code: #150159
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CAS Number 934164-55-3

science Other reagents with same CAS 934164-55-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 396.91 g/mol
Formula C₁₇H₃₃ClN₂O₆
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of targeted drug delivery systems. Its structure allows for selective conjugation with biomolecules, making it valuable in creating prodrugs and antibody-drug conjugates (ADCs). The chloro and carbamate functional groups enable controlled linkage to active pharmaceutical ingredients, enhancing stability and bioavailability. Also employed in polymer chemistry to introduce hydrophilic spacers with biodegradable characteristics, useful in designing responsive biomaterials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,450.00
inventory 250mg
10-20 days ฿33,020.00
inventory 1g
10-20 days ฿89,120.00

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tert-Butyl (1-chloro-2-oxo-7,10,13-trioxa-3-azahexadecan-16-yl)carbamate
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Used as a key intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of targeted drug delivery systems. Its structure allows for selective conjugation with biomolecules, making it valuable in creating prodrugs and antibody-drug conjugates (ADCs). The chloro and carbamate functional groups enable controlled linkage to active pharmaceutical ingredients, enhancing stability and bioavailability. Also employed in polymer chemistry to introduce hydrophilic spacers wi

Used as a key intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of targeted drug delivery systems. Its structure allows for selective conjugation with biomolecules, making it valuable in creating prodrugs and antibody-drug conjugates (ADCs). The chloro and carbamate functional groups enable controlled linkage to active pharmaceutical ingredients, enhancing stability and bioavailability. Also employed in polymer chemistry to introduce hydrophilic spacers with biodegradable characteristics, useful in designing responsive biomaterials.

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