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CS-W001157 4
Total: USD 88.00

BC-NH2

  • CAS No. 1004524-64-4

  • Cat. No. CS-0186372
  • Purity≥95%
  • MDL No.MFCD31568524

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

BC-NH2|CS-0186372

Structure of 1004524-64-4

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General Information

  • CAS No. 1004524-64-4
  • Cat. No. CS-0186372
  • Purity ≥95%
  • MDL No. MFCD31568524
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₄N₄O
  • Molecular Weight 230.27
  • Synonym(s) CLIP-NH2
  • SMILES NC1=NC(OCC2=CC=C(CN)C=C2)=NC=C1

Description

This pyrimidine derivative features a strategically positioned aminomethylbenzyl ether moiety, enabling integration into bioconjugation workflows. The dual amine functionality supports modular derivatization, while the electron-rich heterocycle enhances solubility and stability under standard bench conditions.

Application

2-((4-(Aminomethyl)benzyl)oxy)pyrimidin-4-amine serves as a versatile bifunctional building block for medicinal chemistry and API synthesis. The pyrimidine core enables robust coupling reactions, while the pendant aminomethylbenzyl ether offers site-specific derivatization potential. Its stability under standard synthetic conditions and compatibility with diverse functional groups facilitate efficient route optimization in target-oriented synthesis.

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   87.05
  • LogP   1.0965
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   4

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