2-(1-Trityl-1H-imidazol-4-yl)ethanamine

Name: 2-(1-Trityl-1H-imidazol-4-yl)ethanamine
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CAS No. 195053-92-0
Cat. No. CS-W006417
Purity≥98%
MDL No.MFCD06738986

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2-(1-Trityl-1H-imidazol-4-yl)ethanamine|CS-W006417

Structure of 195053-92-0

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General Information

CAS No. 195053-92-0
Cat. No. CS-W006417
Purity ≥98%
MDL No. MFCD06738986
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₂₄H₂₃N₃
Molecular Weight 353.46
Synonym(s) 2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE
SMILES NCCC1=CN(C(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)C=N1

Description

This imidazole derivative features a trityl-protected amine handle, enabling selective functionalization in peptide and oligonucleotide synthesis. The electron-rich imidazolyl core enhances nucleophilicity, while the bulky trityl group provides steric shielding and facilitates purification via precipitation.

Application

2-(1-Trityl-1H-imidazol-4-yl)ethanamine serves as a protected imidazole building block for peptide and heterocyclic synthesis, offering enhanced solubility and stability during iterative coupling steps. The trityl group provides orthogonal protection for the imidazole nitrogen, enabling selective deprotection under mild acidic conditions. This facilitates efficient access to functionalized imidazole scaffolds in medicinal chemistry and combinatorial libraries.

Safety Information

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GHS Pictogram :	GHS No : GHS05
Signal Word : Danger	UN#: 3259
Class : 8	Packing Group : Ⅲ
Hazard Statements : H314-H318
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 43.84
LogP 4.2245
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 6

Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Imidazole compounds

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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2-(1-Trityl-1H-imidazol-4-yl)ethanamine

CAS No. 195053-92-0

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