Catalog Number |
ACM109306210-2 |
CAS |
109306-21-0 |
Structure |
|
Description |
(+)-4,5-Bis[hydroxy(diphenyl)methyl]-2-methyl-2-phenyl-1,3-dioxolane, also known as (+)-BPPM, is a synthetic chiral compound derived from the reaction of (+)-4,5-bis(hydroxymethyl)-2-methyl-2-phenyl-1,3-dioxolane and (+)-2-methyl-2-phenyl-1,3-dioxolane. This compound has been extensively studied for its potential applications in the fields of organic chemistry and medicinal chemistry. It has been used as a chiral auxiliary in asymmetric synthesis and as a building block for the synthesis of various bioactive molecules. In addition, (+)-BPPM has been found to have significant biological activities, including anti-inflammatory, anti-cancer, and anti-microbial effects. |
IUPAC Name |
[(4R,5R)-5-[hydroxy(diphenyl)methyl]-2-methyl-2-phenyl-1,3-dioxolan-4-yl]-diphenylmethanol |
Molecular Weight |
528.6 g/mol |
Molecular Formula |
C36H32O4 |
Canonical SMILES |
CC1(OC(C(O1)C(C2=CC=CC=C2)(C3=CC=CC=C3)O)C(C4=CC=CC=C4)(C5=CC=CC=C5)O)C6=CC=CC=C6 |
InChI |
InChI=1S/C36H32O4/c1-34(27-17-7-2-8-18-27)39-32(35(37,28-19-9-3-10-20-28)29-21-11-4-12-22-29)33(40-34)36(38,30-23-13-5-14-24-30)31-25-15-6-16-26-31/h2-26,32-33,37-38H,1H3/t32-,33-/m1/s1 |
InChI Key |
QVQMFUMIQACODH-CZNDPXEESA-N |
Application |
(+)-BPPM has been extensively studied for its potential applications in the fields of organic chemistry and medicinal chemistry. It has been used as a chiral auxiliary in asymmetric synthesis and as a building block for the synthesis of various bioactive molecules. In addition, (+)-BPPM has been found to have significant biological activities, including anti-inflammatory, anti-cancer, and anti-microbial effects.In organic chemistry, (+)-BPPM has been found to be a highly efficient chiral auxiliary for the asymmetric synthesis of various compounds, including amino acids and peptides. It has also been used for the synthesis of various natural products, such as terpenoids, alkaloids, and steroids.In medicinal chemistry, (+)-BPPM has been used as a building block for the synthesis of various bioactive molecules, such as small-molecule drugs and drug candidates. It has also been used in the synthesis of various prodrugs, which are designed to increase the solubility and bioavailability of drugs. |
Isomeric SMILES |
CC1(O[C@H]([C@@H](O1)C(C2=CC=CC=C2)(C3=CC=CC=C3)O)C(C4=CC=CC=C4)(C5=CC=CC=C5)O)C6=CC=CC=C6 |
Properties |
The biochemical and physiological effects of (+)-BPPM have not been extensively studied. However, it has been found to have anti-inflammatory, anti-cancer, and anti-microbial effects. In addition, it has been found to have anti-oxidant properties, which may be beneficial in the treatment of various diseases and disorders. |