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CS-W001157 4
Total: USD 88.00

Boc-C2-NH2

  • CAS No. 15231-41-1

  • Cat. No. CS-W018756
  • Purity≥98%
  • MDL No.MFCD06212562

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

Boc-C2-NH2|CS-W018756

Structure of 15231-41-1

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General Information

  • CAS No. 15231-41-1
  • Cat. No. CS-W018756
  • Purity ≥98%
  • MDL No. MFCD06212562
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₅NO₂
  • Molecular Weight 145.20
  • Synonym(s) None
  • SMILES O=C(OC(C)(C)C)CCN

Description

Boc-C2-NH2 delivers a protected primary amine functionality with enhanced stability and ease of handling. This bench-stable reagent integrates readily into peptide coupling sequences, enabling efficient incorporation of aminoethyl units. The tert-butoxycarbonyl group ensures reliable protection under standard conditions, while the ethylene spacer provides optimal flexibility for downstream deprotection and functionalization.

Application

Boc-C2-NH2 serves as a versatile building block for the synthesis of amino acid derivatives and bioactive peptides. The tert-butyl carbamate (Boc) group provides excellent stability under basic conditions and facilitates straightforward deprotection with mild acids. Its terminal primary amine enables efficient coupling reactions, while the ethylene linker offers conformational flexibility, making it well-suited for solid-phase peptide synthesis and the construction of heterocyclic scaffolds in medicinal chemistry applications.

Safety Information

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

Quality Control

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Computational Chemistry Data

  • TPSA   52.32
  • LogP   0.6769
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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