((1S,2S,5R)-2-Isopropyl-5-methylcyclohexyl)diphenylphosphine

Catalog Number	ACM43077298
CAS	43077-29-8
Structure
Description	((1S,2S,5R)-2-Isopropyl-5-methylcyclohexyl)diphenylphosphine, hereafter referred to as IPMDP, is an organophosphine compound that has recently been gaining attention due to its potential applications in scientific research. IPMDP is a chiral compound, meaning that it has two different configurations that are mirror images of each other and cannot be superimposed. This gives IPMDP unique properties that make it useful in a variety of scientific applications. This paper will discuss the synthesis method, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and potential future directions for IPMDP.
IUPAC Name	[(1S,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl]-diphenylphosphane
Molecular Weight	324.4 g/mol
Molecular Formula	C22H29P
Canonical SMILES	CC1CCC(C(C1)P(C2=CC=CC=C2)C3=CC=CC=C3)C(C)C
InChI	InChI=1S/C22H29P/c1-17(2)21-15-14-18(3)16-22(21)23(19-10-6-4-7-11-19)20-12-8-5-9-13-20/h4-13,17-18,21-22H,14-16H2,1-3H3/t18-,21+,22+/m1/s1
InChI Key	BEYDOEXXFGNVRZ-COPCDDAFSA-N
Application	IPMDP has a variety of potential applications in scientific research. It has been used in the synthesis of chiral molecules, as well as in the synthesis of other organophosphines. IPMDP has also been used as a catalyst in asymmetric hydrogenation reactions, and as a reagent in the synthesis of organic compounds. In addition, IPMDP has been used to study the structure and reactivity of organophosphines.
Isomeric SMILES	C[C@@H]1CC[C@H]([C@H](C1)P(C2=CC=CC=C2)C3=CC=CC=C3)C(C)C
Properties	The biochemical and physiological effects of IPMDP are not well understood. However, IPMDP has been shown to interact with proteins in a variety of ways, including through covalent bonding and non-covalent interactions. It has also been shown to interact with DNA and RNA, and to affect the activity of enzymes. In addition, IPMDP has been shown to induce apoptosis in cancer cells.