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CS-W001157 4
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Allyl (2-aminoethyl)carbamate hydrochloride

  • CAS No. 1049722-41-9

  • Cat. No. CS-0151406
  • Molecule weight180.63
  • Purity≥98%
  • MDL No.MFCD05865258

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

Allyl (2-aminoethyl)carbamate hydrochloride|CS-0151406

Structure of 1049722-41-9

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General Information

  • CAS No. 1049722-41-9
  • Cat. No. CS-0151406
  • Purity ≥98%
  • MDL No. MFCD05865258
  • Storage RT, stored under nitrogen, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₁₃ClN₂O₂
  • Molecular Weight 180.63
  • Synonym(s) None
  • SMILES O=C(OCC=C)NCCN.Cl

Description

Allyl (2-aminoethyl)carbamate (hydrochloride) features a reactive allyl group paired with a primary amine and carbamate functionality, enabling facile conjugation in bioorthogonal workflows. This bench-stable derivative supports efficient incorporation into peptide and polymer architectures under mild conditions.

Application

Allyl (2-aminoethyl)carbamate (hydrochloride) serves as a versatile bifunctional building block for peptide and peptidomimetic synthesis, enabling efficient introduction of allyl-protected amine handles. Its stability under standard reaction conditions facilitates orthogonal deprotection strategies, while the carbamate linkage offers reliable conjugation compatibility. The hydrochloride salt enhances solubility and handling in aqueous and polar organic media, supporting scalable applications in medicinal chemistry and combinatorial synthesis workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 1759
Class : 8
Packing Group : Ⅲ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

  • TPSA   64.35
  • LogP   0.2791
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   4

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