754201-24-6

Basic information

• Product Name: (Z)-(4R,6R,8R)-17,19-Bis-methoxymethoxy-4-methyl-12-phenylsulfanyl-3,7-dioxa-tricyclo[13.4.0.0^6,8]nonadeca-1⁽¹⁹⁾,9,15,17-tetraene-2,13-dione
• Synonyms: (Z)-(4R,6R,8R)-17,19-Bis-methoxymethoxy-4-methyl-12-phenylsulfanyl-3,7-dioxa-tricyclo[13.4.0.0^6,8]nonadeca-1⁽¹⁹⁾,9,15,17-tetraene-2,13-dione
• CAS NO: 754201-24-6
• Molecular Weight: 528.623
• Mol File: 754201-24-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (Z)-(4R,6R,8R)-17,19-Bis-methoxymethoxy-4-methyl-12-phenylsulfanyl-3,7-dioxa-tricyclo[13.4.0.0^6,8]nonadeca-1⁽¹⁹⁾,9,15,17-tetraene-2,13-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-(4R,6R,8R)-17,19-Bis-methoxymethoxy-4-methyl-12-phenylsulfanyl-3,7-dioxa-tricyclo[13.4.0.0^6,8]nonadeca-1⁽¹⁹⁾,9,15,17-tetraene-2,13-dione(754201-24-6)
• EPA Substance Registry System: (Z)-(4R,6R,8R)-17,19-Bis-methoxymethoxy-4-methyl-12-phenylsulfanyl-3,7-dioxa-tricyclo[13.4.0.0^6,8]nonadeca-1⁽¹⁹⁾,9,15,17-tetraene-2,13-dione(754201-24-6)

Safety Data

• Hazardous Substances Data: 754201-24-6(Hazardous Substances Data)

Upstream product

• 378749-88-3 (3R,4R,6S)-6-(hydroxy)-3,4-(oxiranyl)hept-1-ene 
• 754201-18-8 (3S,4R,6S)-6-(tert-Butyl-diphenyl-silanyloxy)-3-phenylsulfanyl-hept-1-en-4-ol 
• 378750-02-8 (3R,4R,6S)-6-(tert-butyldiphenylsilyl)-3,4-(oxiranyl)hept-1-ene 
• 867367-94-0 2,4-Dihydroxy-6-methyl-benzoic acid (R)-1-methyl-2-((2R,3R)-3-vinyl-oxiranyl)-ethyl ester 
• 480-64-8 orsellinic acid 
• 867367-83-7 2,4-Bis-methoxymethoxy-6-methyl-benzoic acid (R)-1-methyl-2-((2R,3R)-3-vinyl-oxiranyl)-ethyl ester 
• 754201-16-6 N-methoxy-N-methyl-2-(phenylthio)pent-4-enamide 
• 191731-37-0 N-methoxy-N-methyl-2-(phenylthio)acetamide 
• 108-98-5 thiophenol 
• 867367-84-8 2,4-Bis-methoxymethoxy-6-(2-oxo-3-phenylsulfanyl-hex-5-enyl)-benzoic acid (R)-1-methyl-2-((2R,3R)-3-vinyl-oxiranyl)-ethyl ester 

Downstream Products

• 12772-57-5 (9Z,11E)-(4R,6R,8R)-16-Chloro-17,19-dihydroxy-4-methyl-3,7-dioxa-tricyclo[13.4.0.0^6,8]nonadeca-1⁽¹⁵⁾,9,11,16,18-pentaene-2,13-dione 

Relevant articles and documents

Modular asymmetric synthesis of pochonin C

Back to its origins: Pochonin C was synthesized in 11 steps from the four fragments shown in the scheme. This asymmetric synthesis and the conversion of pochonin C into radicicol defines the configuration at the center bearing the chlorine atom as S. lpc