(4R,4'R)-2,2'-(Propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)

Catalog Number	ACM141362778-2
CAS	141362-77-8
Structure
Description	(4R,4'R)-2,2'-(Propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) is a synthetic compound that has been developed for a variety of scientific research applications. It is a benzylated oxazole derivative that is composed of two propane-2,2-diyl moieties and two benzyl substituents on the 4 and 4' positions of the oxazole ring. This compound is known for its ability to act as a catalyst for a variety of reactions, as well as its ability to act as an inhibitor for certain enzymes.
IUPAC Name	(4R)-4-benzyl-2-[2-[(4R)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]propan-2-yl]-4,5-dihydro-1,3-oxazole
Molecular Weight	362.5 g/mol
Molecular Formula	C23H26N2O2
Canonical SMILES	CC(C)(C1=NC(CO1)CC2=CC=CC=C2)C3=NC(CO3)CC4=CC=CC=C4
InChI	InChI=1S/C23H26N2O2/c1-23(2,21-24-19(15-26-21)13-17-9-5-3-6-10-17)22-25-20(16-27-22)14-18-11-7-4-8-12-18/h3-12,19-20H,13-16H2,1-2H3/t19-,20-/m1/s1
InChI Key	GAKCKAKYRQUVRK-WOJBJXKFSA-N
Application	(4R,4'R)-2,2'-(Propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) has been used in a variety of scientific research applications. It has been studied for its ability to act as a catalyst for a variety of chemical reactions, such as the synthesis of novel heterocyclic compounds and the preparation of polymers. Additionally, it has been studied as an inhibitor for certain enzymes, such as the enzyme cyclooxygenase.
GHS Pictogram	Irritant
Isomeric SMILES	CC(C)(C1=N[C@@H](CO1)CC2=CC=CC=C2)C3=N[C@@H](CO3)CC4=CC=CC=C4
Properties	The biochemical and physiological effects of (4R,4'R)-2,2'-(Propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) have not been extensively studied. However, it is known to have a low level of toxicity and has been found to be non-mutagenic. Additionally, it has been shown to have some anti-inflammatory properties.