78606-81-2

Basic information

• Product Name: Benzoic acid (2Z,5Z)-(S)-1-(3-methoxycarbonyl-propyl)-6-[(2R,3R)-((Z)-3-oct-2-enyl)-oxiranyl]-hexa-2,5-dienyl ester
• Synonyms: Benzoic acid (2Z,5Z)-(S)-1-(3-methoxycarbonyl-propyl)-6-[(2R,3R)-((Z)-3-oct-2-enyl)-oxiranyl]-hexa-2,5-dienyl ester
• CAS NO: 78606-81-2
• Molecular Weight: 454.607
• Mol File: 78606-81-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid (2Z,5Z)-(S)-1-(3-methoxycarbonyl-propyl)-6-[(2R,3R)-((Z)-3-oct-2-enyl)-oxiranyl]-hexa-2,5-dienyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid (2Z,5Z)-(S)-1-(3-methoxycarbonyl-propyl)-6-[(2R,3R)-((Z)-3-oct-2-enyl)-oxiranyl]-hexa-2,5-dienyl ester(78606-81-2)
• EPA Substance Registry System: Benzoic acid (2Z,5Z)-(S)-1-(3-methoxycarbonyl-propyl)-6-[(2R,3R)-((Z)-3-oct-2-enyl)-oxiranyl]-hexa-2,5-dienyl ester(78606-81-2)

Safety Data

• Hazardous Substances Data: 78606-81-2(Hazardous Substances Data)

Upstream product

• 76745-19-2 (5S,6R)-Methyl 5-(benzyloxy)-6,7-dihydroxyheptanoate 
• 78606-79-8 Benzoic acid (S)-4-methoxycarbonyl-1-(R)-oxiranyl-butyl ester 
• 78606-78-7 methyl (E,5S,6R)-5,6,7-trihydroxyhept-2-enoate 
• 78606-80-1 5(S), 6(R), 7-trihydroxyheptanoic acid methyl ester 
• 86421-16-1 2,3-oxido-undeca-2-trans-5-cis-dien-1-ol 
• 76793-15-2 (2R,3R)-((Z)-3-Oct-2-enyl)-oxirane-2-carbaldehyde 
• 76745-17-0 (5S,6R)-5,6-Dihydroxy-7-(toluene-4-sulfonyloxy)-heptanoic acid methyl ester 
• 78606-75-4 (2R,3R)-2-[(Z)-4-(1-Methoxy-1-methyl-ethoxy)-but-1-enyl]-3-((Z)-oct-2-enyl)-oxirane 
• 78606-76-5 (Z)-4-[(2R,3R)-((Z)-3-Oct-2-enyl)-oxiranyl]-but-3-en-1-ol 
• 76745-20-5 Methyl 5S-benzoyloxy-5-formylvalerate 
• 78606-77-6 {(Z)-4-[(2R,3R)-((Z)-3-Oct-2-enyl)-oxiranyl]-but-3-enyl}-triphenyl-phosphonium; iodide 

Downstream Products

• 71160-24-2 Leukotriene B 

Relevant articles and documents

A STEREOCONTROLLED AND EFFECTIVE SYNTHESIS OF LEUKOTRIENE B (1).

An efficient synthesis of leukotriene B (1) is reported which renders this important substance accessible in quantity.The process is convergent and includes a novel method for stereospecific generation of the conjugated triene unit.