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CS-W001157 4
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Allyl (2-bromoethyl)carbamate

  • CAS No. 347372-90-1

  • Cat. No. CS-0697868
  • Molecule weight208.05
  • Purity≥95%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

Allyl (2-bromoethyl)carbamate|CS-0697868

Structure of 347372-90-1

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General Information

  • CAS No. 347372-90-1
  • Cat. No. CS-0697868
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₁₀BrNO₂
  • Molecular Weight 208.05
  • Synonym(s) None
  • SMILES BrCCNC(=O)OCC=C

Description

Allyl (2-bromoethyl)carbamate features a reactive allyl group paired with a bromoethyl carbamate moiety, enabling efficient conjugation in synthetic workflows. This bifunctional reagent integrates seamlessly into click chemistry and peptide modification strategies, offering high chemoselectivity under mild conditions. The molecule's stability facilitates handling while maintaining reactivity for downstream transformations.

Application

Allyl (2-bromoethyl)carbamate serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient introduction of both allyl and bromoethyl functionalities. It functions as a protected amine synthon with orthogonal reactivity, facilitating subsequent transformations such as nucleophilic substitution, palladium-catalyzed coupling, and ring-opening reactions. The allyl group allows for convenient removal via Pd(0)-mediated deprotection, while the bromoethyl moiety supports further functionalization through SN2 processes. Its stability under standard bench conditions and compatibility with diverse reaction environments make it well-suited for complex molecule synthesis, including peptide analogs and heterocyclic scaffolds.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   38.33
  • LogP   1.2935
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   4

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