2-(2-((tert-Butoxycarbonyl)amino)ethoxy)ethyl 4-methylbenzenesulfonate

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Reagent Code: #81975
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CAS Number 192132-77-7

science Other reagents with same CAS 192132-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.44 g/mol
Formula C₁₆H₂₅NO₆S
badge Registry Numbers
MDL Number MFCD28506265
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a protective group reagent. It is often employed to protect amines during complex chemical reactions, ensuring that the amine group remains unaffected while other functional groups undergo transformation. The tert-butoxycarbonyl (Boc) group attached to the amine provides stability under various reaction conditions, making it suitable for multi-step synthesis processes. Additionally, the tosylate group in the molecule serves as a good leaving group, facilitating nucleophilic substitution reactions. This compound is particularly valuable in the synthesis of peptides, pharmaceuticals, and other biologically active molecules where selective protection and deprotection of functional groups are critical. Its application extends to the development of drug intermediates and fine chemicals, where precise control over reaction pathways is essential.

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Test Parameter Specification
Appearance White Solid
Purity (%) 97.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,260.00
inventory 1g
10-20 days ฿3,177.00
inventory 5g
10-20 days ฿11,079.00

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2-(2-((tert-Butoxycarbonyl)amino)ethoxy)ethyl 4-methylbenzenesulfonate
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This chemical is primarily utilized in organic synthesis as a protective group reagent. It is often employed to protect amines during complex chemical reactions, ensuring that the amine group remains unaffected while other functional groups undergo transformation. The tert-butoxycarbonyl (Boc) group attached to the amine provides stability under various reaction conditions, making it suitable for multi-step synthesis processes. Additionally, the tosylate group in the molecule serves as a good leaving group, facilitating nucleophilic substitution reactions. This compound is particularly valuable in the synthesis of peptides, pharmaceuticals, and other biologically active molecules where selective protection and deprotection of functional groups are critical. Its application extends to the development of drug intermediates and fine chemicals, where precise control over reaction pathways is essential.
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