Bis(2-((S)-4-phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine

Name: Bis(2-((S)-4-phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine
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CAS No. 485394-21-6
Cat. No. CS-0131851
Purity≥97%
MDL No.None

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Bis(2-((S)-4-phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine|CS-0131851

Structure of 485394-21-6

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General Information

CAS No. 485394-21-6
Cat. No. CS-0131851
Purity ≥97%
MDL No. None
Storage -20°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₃₀H₂₅N₃O₂
Molecular Weight 459.54
Synonym(s) 2-[(4S)-4,5-Dihydro-4-phenyl-2-oxazolyl]-N-[2-[(4S)-4,5-dihydro-4-phenyl-2-oxazolyl]phenyl]benzenamine
SMILES C1(NC2=CC=CC=C2C3=N[C@@H](C4=CC=CC=C4)CO3)=CC=CC=C1C5=N[C@@H](C6=CC=CC=C6)CO5

Description

Bis(2-((S)-4-phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine features a chiral oxazoline scaffold flanked by aryl groups, enabling precise stereochemical control in asymmetric synthesis. The amine moiety integrates readily into catalytic frameworks, while the electron-rich aromatic system enhances stability and coordination versatility. This structure supports efficient ligand design for transition-metal catalysis under ambient conditions.

Application

Bis(2-((S)-4-phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine serves as a robust chiral ligand scaffold in transition metal catalysis, enabling asymmetric transformations through well-defined coordination sites. Its dihydrooxazoline moieties provide enhanced stereocontrol and stability under standard reaction conditions, facilitating efficient C–C and C–heteroatom bond formations. The molecule exhibits excellent bench stability, simplifies purification, and demonstrates broad functional group tolerance in established synthetic workflows.

Safety Information

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GHS Pictogram :	GHS No : GHS09
Signal Word : Warning	UN#: 3077
Class : 9	Packing Group : Ⅲ
Hazard Statements : H410
Precautionary Statements : P273-P391-P501

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Computational Chemistry Data

TPSA 55.21
LogP 6.4664
H_Acceptors 5
H_Donors 1
Rotatable_Bonds 6

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Bis(2-((S)-4-phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine

CAS No. 485394-21-6

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