tert-Butyl (23-hydroxy-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate

95%

Reagent Code: #61602
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CAS Number 1345337-22-5

science Other reagents with same CAS 1345337-22-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 469.57 g/mol
Formula C₂₁H₄₃NO₁₀
badge Registry Numbers
MDL Number MFCD28976659
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of drug development and medicinal chemistry. It serves as a protective group for amines during multi-step synthetic processes, ensuring selective reactions without unwanted side interactions. Its structure, featuring a long polyether chain, enhances solubility in various solvents, making it suitable for reactions in both organic and aqueous environments. Additionally, it is employed in the preparation of peptide-based therapeutics, where its stability under mild conditions allows for efficient deprotection without disrupting the peptide backbone. Its applications also extend to the development of advanced materials, such as polymers and dendrimers, where its functional groups enable precise modifications and controlled assembly.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿16,416.00
inventory 5g
10-20 days ฿57,447.00
inventory 250mg
10-20 days ฿6,570.00

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tert-Butyl (23-hydroxy-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate
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This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of drug development and medicinal chemistry. It serves as a protective group for amines during multi-step synthetic processes, ensuring selective reactions without unwanted side interactions. Its structure, featuring a long polyether chain, enhances solubility in various solvents, making it suitable for reactions in both organic and aqueous environments. Additionally, it is employed in the prepara

This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of drug development and medicinal chemistry. It serves as a protective group for amines during multi-step synthetic processes, ensuring selective reactions without unwanted side interactions. Its structure, featuring a long polyether chain, enhances solubility in various solvents, making it suitable for reactions in both organic and aqueous environments. Additionally, it is employed in the preparation of peptide-based therapeutics, where its stability under mild conditions allows for efficient deprotection without disrupting the peptide backbone. Its applications also extend to the development of advanced materials, such as polymers and dendrimers, where its functional groups enable precise modifications and controlled assembly.

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