(4S,4'S,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]

Name: (4S,4'S,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]
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CAS No. 529489-04-1
Cat. No. CS-0097366
Purity≥97%
MDL No.None

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(4S,4'S,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]|CS-0097366

Structure of 529489-04-1

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General Information

CAS No. 529489-04-1
Cat. No. CS-0097366
Purity ≥97%
MDL No. None
Storage -20°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₃₃H₃₀N₂O₂
Molecular Weight 486.60
Synonym(s) (4S,5S,4'S,5'S)-2,2'-(2,2-Propanediyl)bis(4,5-diphenyl-4,5-dihydro-1,3-oxazole)
SMILES CC(C1=N[C@@H](C2=CC=CC=C2)[C@H](C3=CC=CC=C3)O1)(C)C4=N[C@@H](C5=CC=CC=C5)[C@H](C6=CC=CC=C6)O4

Description

(S,S)-BisPh-propabBox features a chiral bis(phenyl)propylene scaffold with tailored steric and electronic properties, enabling high enantioselectivity in asymmetric catalysis. This bench-stable ligand integrates seamlessly into transition-metal complexes for stereoselective transformations under standard conditions.

Application

(S,S)-BisPh-propabBox serves as a robust, bench-stable chiral ligand for asymmetric catalysis, enabling high enantioselectivity in transition-metal-catalyzed transformations. Its rigid propylene-bridged bisphosphine architecture provides excellent stereocontrol and functional group tolerance, facilitating efficient synthesis of chiral intermediates in medicinal chemistry and process development.

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

TPSA 43.18
LogP 7.8352
H_Acceptors 4
H_Donors 0
Rotatable_Bonds 6

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(4S,4'S,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]

CAS No. 529489-04-1

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