76686-31-2

Basic information

• Product Name: [(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride
• Synonyms: [(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride
• CAS NO: 76686-31-2
• Molecular Weight: 517.091
• Mol File: 76686-31-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: [(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride(76686-31-2)
• EPA Substance Registry System: [(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride(76686-31-2)

Safety Data

• Hazardous Substances Data: 76686-31-2(Hazardous Substances Data)

Usage

General Description

[(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride is a chemical compound with the molecular formula C38H40ClO2P. It is a salt containing a phosphonium cation and a chloride anion. The compound is characterized by a long hydrophobic tail and a hydrophilic head group, making it useful in lipid-based drug delivery systems. It is also known to have antioxidant properties and has potential applications in pharmaceuticals and biotechnology. The compound is derived from a naturally occurring carotenoid and is a vital component in the development of pharmaceutical and therapeutic products.

Upstream product

• 54165-55-8 (3R)-3-Acetoxy-β-ionon 
• 116296-75-4 (rac)-(E)-4-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one 
• 38963-41-6 (rac)-4-(4-hydroxy-2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one 

Downstream Products

• 472-70-8 (3R)-cryptoxanthin 
• 62742-02-3 (all-E)-(3R)-3-hydroxy-12'-apo-β-caroten-12'-al 
• 1027012-24-3 (R)-4-[(1E,3E,5E,7E,9E,11E)-12-(5,5-Dimethyl-[1,3]dioxan-2-yl)-3,7-dimethyl-trideca-1,3,5,7,9,11-hexaenyl]-3,5,5-trimethyl-cyclohex-3-enol 
• 23984-55-6 (3R,6'RS)-3-hydroxy-β,ε-caroten-3'-one 
• 144-68-3 zeaxanthin 
• 136734-01-5 (7Z,3R,3'R)-zeaxanthin 

Relevant articles and documents

Synthesis of (3S)- and (3R)-3-hydroxy-β-ionone and their transformation into (3S)- and (3R)-β- cryptoxanthin

(3S)- and (3R)-3-Hydroxy-β-ionone and (3S)- and (3R)-3-Hydroxy-β- ionone synthesized in high enantiomeric purity from commercially available () - ionone. These ionones were then transformed into (3R) - cryptoxanthin and (3S) - cryptoxanthin by a C15+C10+C15 Wittig coupling strategy according to known methods. This methodology can considerably simplify the total synthesis of optically active carotenoids with 3-hydroxy - end groups that possess significant biological activities. Georg Thieme Verlag Stuttgart New York.