tert-Butyl (2-(2-(2-(prop-2-yn-1-yloxy)ethoxy)ethoxy)ethyl)carbamate

95%

  • Product Code: 61596
  CAS:    1333880-60-6
Molecular Weight: 287.35 g./mol Molecular Formula: C₁₄H₂₅NO₅
EC Number: MDL Number: MFCD30534430
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, sealed, dry
Product Description: This chemical is primarily utilized in organic synthesis and pharmaceutical research as a versatile building block. It is often employed in the development of complex molecules, particularly in the synthesis of peptide-based compounds and drug candidates. The presence of the tert-butyl carbamate group provides protection for amine functionalities during chemical reactions, ensuring selective transformations. Additionally, the prop-2-yn-1-yloxy moiety allows for further functionalization through click chemistry, making it valuable in the design of targeted drug delivery systems and bioconjugation strategies. Its application extends to the creation of advanced materials and polymers, where its structure contributes to the development of tailored properties.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $158.21
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1.000 10-20 days $395.53
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5.000 10-20 days $1,384.13
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tert-Butyl (2-(2-(2-(prop-2-yn-1-yloxy)ethoxy)ethoxy)ethyl)carbamate
This chemical is primarily utilized in organic synthesis and pharmaceutical research as a versatile building block. It is often employed in the development of complex molecules, particularly in the synthesis of peptide-based compounds and drug candidates. The presence of the tert-butyl carbamate group provides protection for amine functionalities during chemical reactions, ensuring selective transformations. Additionally, the prop-2-yn-1-yloxy moiety allows for further functionalization through click chemistry, making it valuable in the design of targeted drug delivery systems and bioconjugation strategies. Its application extends to the creation of advanced materials and polymers, where its structure contributes to the development of tailored properties.
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