1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine

Name: 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine
Brand: ChemScene
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CAS No. 1225062-60-1
Cat. No. CS-0030775
Purity≥97%
MDL No.MFCD18383321

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FedEx Limited Quantities Ground	$0.00
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1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine|CS-0030775

Structure of 1225062-60-1

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General Information

CAS No. 1225062-60-1
Cat. No. CS-0030775
Purity ≥97%
MDL No. MFCD18383321
Storage -20°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₇H₂₄BNO₂
Molecular Weight 285.19
Synonym(s) 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-1,2,3,6-tetrahydropyridine
SMILES CC(C(C)(C)O1)(C)OB1C2=CCN(CC2)C3=CC=CC=C3

Description

1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine features a boronate ester group enabling efficient Suzuki-Miyaura coupling. The dihydropyridine core provides a stable, electron-rich scaffold for transition metal-catalyzed transformations. This bench-stable reagent integrates seamlessly into C–C bond formation workflows.

Application

1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine serves as a versatile boronate building block in palladium-catalyzed cross-coupling reactions. The dihydro-pyridine core provides a stable, bench-accessible scaffold with excellent functional group tolerance, enabling efficient C–C bond formation under mild conditions. Its tetramethyl-substituted boronate moiety ensures high stability and compatibility with aqueous workups, facilitating purification and integration into complex molecular architectures.

Safety Information

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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-P330-P362+P364-P405-P501

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Computational Chemistry Data

TPSA 21.7
LogP 3.4545
H_Acceptors 3
H_Donors 0
Rotatable_Bonds 2

Other Classifications

Building Blocks Skeleton Aliphatic heterocycle compounds Piperidine compounds

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine

CAS No. 1225062-60-1

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