[2,2':6',2''-Terpyridin]-4'-ylmethanol

Name: [2,2':6',2''-Terpyridin]-4'-ylmethanol
Brand: ChemScene
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CAS No. 148332-32-5
Cat. No. CS-0371262
Purity≥98%
MDL No.MFCD14636293

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[2,2':6',2''-Terpyridin]-4'-ylmethanol|CS-0371262

Structure of 148332-32-5

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General Information

CAS No. 148332-32-5
Cat. No. CS-0371262
Purity ≥98%
MDL No. MFCD14636293
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₆H₁₃N₃O
Molecular Weight 263.30
Synonym(s) 4'-Hydroxymethyl-2,2':6',2''-terpyridine
SMILES OCC1=CC(C2=CC=CC=N2)=NC(C3=NC=CC=C3)=C1

Description

This terpyridine derivative features a hydroxymethyl group at the 4′-position, enabling direct functionalization or conjugation in coordination chemistry. The extended π-system delivers strong metal-chelating affinity, while the pendant alcohol facilitates solubility and downstream derivatization. Designed for use in catalytic complexes, molecular assemblies, and surface immobilization applications.

Application

[2,2':6',2''-Terpyridin]-4'-ylmethanol serves as a versatile ligand building block in transition metal catalysis and coordination chemistry. Its pyridine-rich architecture enables strong chelation with late transition metals, while the pendant primary alcohol facilitates downstream functionalization via esterification, etherification, or immobilization. Bench-stable and readily purified by recrystallization, it functions effectively in homogeneous catalytic systems and supramolecular assemblies.

Safety Information

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GHS Pictogram : N/A	GHS No : N/A
Signal Word : N/A	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

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Computational Chemistry Data

TPSA 58.9
LogP 2.6979
H_Acceptors 4
H_Donors 1
Rotatable_Bonds 3

Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Key Words

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[2,2':6',2''-Terpyridin]-4'-ylmethanol

CAS No. 148332-32-5

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