600180-00-5

Basic information

• Product Name: Benzene, [[[(1S,2E,4Z)-7-iodo-1-pentyl-2,4-heptadienyl]oxy]methyl]-
• CAS NO: 600180-00-5
• Molecular Formula: C19H27IO
• Molecular Weight: 398.327
• Mol File: 600180-00-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzene, [[[(1S,2E,4Z)-7-iodo-1-pentyl-2,4-heptadienyl]oxy]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [[[(1S,2E,4Z)-7-iodo-1-pentyl-2,4-heptadienyl]oxy]methyl]-(600180-00-5)
• EPA Substance Registry System: Benzene, [[[(1S,2E,4Z)-7-iodo-1-pentyl-2,4-heptadienyl]oxy]methyl]-(600180-00-5)

Safety Data

• Hazardous Substances Data: 600180-00-5(Hazardous Substances Data)

Upstream product

• 600179-98-4 1-[7-benzyloxy-(3Z,5E,7S)-3,5-dodecadienyloxymethyl]-4-methoxybenzene 
• 600179-97-3 12-(4-methoxybenzyloxy)-1-pentyl (1S,2E,4Z)-2,4-heptadienyl alcohol 
• 392333-43-6 7-hydroxy-(3Z,5E,7S)-3,5-dodecadienyl 5-hydroxypentanoate 
• 392333-39-0 (3Z,6Z)-3,6-dodecadienyl 5-hydroxypentanoate 
• 100-51-6 benzyl alcohol 
• 124099-42-9 (3Z,5E,7S)-3,5-dodecadiene-1,7-diol 
• 4257-83-4 benzyl 2,2,2-trichloroacetamide 
• 600179-99-5 7-benzyloxy-(3Z,5E,7S)-3,5-dodecadiene-1-ol 

Downstream Products

• 1026888-20-9 2-((8Z,11Z,13E)-(S)-15-Benzyloxy-icosa-8,11,13-trienyloxy)-tetrahydro-pyran 
• 600180-04-9 15-benzyloxy-(8Z,11Z,13E,15S)-8,11,13-eicosatrienoic acid 
• 600180-03-8 15-benzyloxy-(8Z,11Z,13E,15S)-8,11,13-eicosatriene-1-ol 
• 600180-02-7 13-benzyloxy-(6Z,9Z,11E,13S)-6,9,11-octadecatrienoic acid 
• 600180-01-6 13-benzyloxy-(6Z,9Z,11E,13S)-6,9,11-octadecatriene-1-ol 
• 74784-20-6 (13S,6Z,9Z,11E)-hydroxyoctadeca-6,9,11-trienoic acid 
• 92693-02-2 15(S)-hydroxyeicosatrienoic acid 

Relevant articles and documents

Asymmetric synthesis of unnatural (Z,Z,E)-octadecatrienoid and eicosatrienoid by lipoxygenase-catalyzed oxygenation

The asymmetric synthesis of unnatural 13-hydroxy-(6Z,9Z,11E,13S)-octadecatrienoid and 15-hydroxy-(8Z,11Z,13E,15S)-eicosatrienoid is described using a biomimetic oxidation route. The main highlights of this synthesis are the asymmetric hydroxylation of the substrate with soybean lipoxygenase and cis selective Wittig olefination.