1027311-89-2

Basic information

• Product Name: (2R,3S)-1-((6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)-3-hydroxy-7-((4-methoxybenzyl)oxy)-2-methylheptan-1-one
• Synonyms: (2R,3S)-1-((6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)-3-hydroxy-7-((4-methoxybenzyl)oxy)-2-methylheptan-1-one
• CAS NO: 1027311-89-2
• Molecular Weight: 493.665
• Mol File: 1027311-89-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S)-1-((6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)-3-hydroxy-7-((4-methoxybenzyl)oxy)-2-methylheptan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-1-((6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)-3-hydroxy-7-((4-methoxybenzyl)oxy)-2-methylheptan-1-one(1027311-89-2)
• EPA Substance Registry System: (2R,3S)-1-((6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)-3-hydroxy-7-((4-methoxybenzyl)oxy)-2-methylheptan-1-one(1027311-89-2)

Safety Data

• Hazardous Substances Data: 1027311-89-2(Hazardous Substances Data)

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 131375-63-8 5-(4-methoxybenzyloxy)-1-pentanol 
• 125664-95-1 N-propionyl-(2R)-bornane-(10,2)-sultam 
• 131375-69-4 5-((4-methoxybenzyl)oxy)pentanal 
• 111-29-5 1 ,5-pentanediol 

Downstream Products

• 935457-57-1 (4S,5S)-9-((4-methoxybenzyl)oxy)-2,4-dimethylnon-1-en-5-ol 
• 935457-60-6 triethyl{(1S,2S)-1-[4'-((4-methoxybenzyl)oxy)butyl]-2,4-dimethylpent-4-enyloxy}silane 
• 935457-52-6 (5S,6S)-((2S,3R)-2-methyl-1-(tosyloxy)hex-5-en-3-yl)-6,8-dimethyl-5-(triethylsilyloxy)non-8-enoate 
• 1001861-38-6 (2S,3S)-7-(4-methoxybenzyloxy)-2-methylheptane-1,3-diol 
• 124224-04-0 (-)-10,2-camphorsultam 
• 935457-56-0 (2S,3S)-3-hydroxy-7-((4-methoxybenzyl)oxy)-2-methylheptyl 4-methylbenzenesulfonate 
• 1352927-85-5 (2S,3S)-2-(4-(4-methoxybenzyloxy)butyl)-3-methyloxetane 

Relevant articles and documents

A ring-closing metathesis (RCM)-based approach to mycolactonesa A/B

The total synthesis of the mycobacterial toxins mycolactones A/B (1 a/b) has been accomplished based on a strategy built around the construction of the mycolactone core through ring-closing metathesis. By employing the Grubbs second-generation catalyst, t