177167-80-5

Basic information

• Product Name: (R)-1-Hexadecyloxy-3-trityloxy-propane-2-thiol
• Synonyms: (R)-1-Hexadecyloxy-3-trityloxy-propane-2-thiol
• CAS NO: 177167-80-5
• Molecular Weight: 574.912
• Mol File: 177167-80-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-1-Hexadecyloxy-3-trityloxy-propane-2-thiol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-Hexadecyloxy-3-trityloxy-propane-2-thiol(177167-80-5)
• EPA Substance Registry System: (R)-1-Hexadecyloxy-3-trityloxy-propane-2-thiol(177167-80-5)

Safety Data

• Hazardous Substances Data: 177167-80-5(Hazardous Substances Data)

Upstream product

• 92471-46-0 (R)-3-(1-hexadecyloxy)-1-(trityloxy)propan-2-ol 
• 506-03-6 chimyl alcohol 
• 89496-73-1 4-(n-hexadecyloxymethyl)-2,2-dimethyl-1,3-dioxolane 
• 6140-88-1 hexadecane-1-sulfonic acid 
• 57959-37-2 3-O-hexadecyl-1,2-O-isopropylidene-sn-glycerol 
• 92445-87-9 (S)-3-(1-hexadecyloxy)-1-(trityloxy)propan-2-yl methanesulfonate 
• 96093-53-7 (S)-3-(1-hexadecyloxy)-1-(trityloxy)propan-2-ol 
• 20779-14-0 methanesulfonic acid hexadecyl ester 
• 10550-58-0 (R)-3-(hexadecyloxy)-1,2-propanediol 
• 177167-79-2 Thioacetic acid S-((R)-1-hexadecyloxymethyl-2-trityloxy-ethyl) ester 

Downstream Products

• 96801-55-7 1-O-hexadecyl-2-deoxy-2-thio-S-acetyl-sn-glyceryl-3-phosphorylcholine 
• 177167-83-8 1-O-hexadecyl-2-S-trityl-sn-2-thioglycero-3-O-phosphocholine 
• 177167-82-7 2-((R)-3-Hexadecyloxy-2-tritylsulfanyl-propoxy)-[1,3,2]dioxaphospholane 2-oxide 
• 146797-82-2 1-O-hexadecyl-2-thioarachidonyl-2-deoxy-sn-glycero-3-phosphocholine 
• 177167-81-6 (S)-3-Hexadecyloxy-2-tritylsulfanyl-propan-1-ol 
• 195832-36-1 (S)-2-Benzylsulfanyl-3-hexadecyloxy-propan-1-ol 

Relevant articles and documents

Platelet activating factor derivative and synthesis method thereof

The invention belongs to the technical field of chemical synthesis and discloses a platelet activating factor derivative with a formula (I) structure, wherein a substituent group R refers to an acryl group. A synthetic route includes nine-step reaction by taking chiral source S-configuration solketal as a starting reactant. The method is adopted for synthesis of a 2-sulfo platelet activating factor and a derivative thereof for the first time and has advantages of high yield, easiness in separation and the like. Low-cost batch synthesis of 2-S-PAF and the derivative thereof is realized, and significances to activity research of 2-S-PAF and the derivative thereof, biological experiments, clinical application and disease treatment are achieved.