179618-61-2

Basic information

• Product Name: 6,8-Dodecadiene-2,3-diol, 12-[(4-methoxyphenyl)methoxy]-2,6-dimethyl-, (E,E)-
• CAS NO: 179618-61-2
• Molecular Formula: C22H34O4
• Molecular Weight: 362.51
• Mol File: 179618-61-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6,8-Dodecadiene-2,3-diol, 12-[(4-methoxyphenyl)methoxy]-2,6-dimethyl-, (E,E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 6,8-Dodecadiene-2,3-diol, 12-[(4-methoxyphenyl)methoxy]-2,6-dimethyl-, (E,E)-(179618-61-2)
• EPA Substance Registry System: 6,8-Dodecadiene-2,3-diol, 12-[(4-methoxyphenyl)methoxy]-2,6-dimethyl-, (E,E)-(179618-61-2)

Safety Data

• Hazardous Substances Data: 179618-61-2(Hazardous Substances Data)

Upstream product

• 83324-69-0 (E)-8-bromo-2,3-O-isopropylidene-2,6-dimethyl-6-octene-2,3-diol 
• 824-94-2 p-methoxybenzyl chloride 
• 179618-58-7 [(E)-3-Methyl-5-(2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-pent-2-enyl]-phosphonic acid diethyl ester 
• 124150-94-3 (E)-3-methyl-5-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)pent-2-en-1-ol 
• 40036-54-2 (E)-5-(3,3-dimethyloxiran-2-yl)-3-methylpent-2-en-1-ol 
• 106-24-1 Geraniol 
• 179618-59-8 5-[(3E,5E)-9-(4-Methoxy-benzyloxy)-3-methyl-nona-3,5-dienyl]-2,2,4,4-tetramethyl-[1,3]dioxolane 
• 119649-27-3 4-((4-methoxybenzyl)oxy)butanal 
• 119649-45-5 4-(p-methoxybenzyloxy)butan-1-ol 

Downstream Products

• 155233-30-0 curacin A 
• 179618-63-4 (4E,6E,10R)-10-hydroxy-1-(4-methoxybenzyl)oxy-7-methyltrideca-4,6,12-triene 
• 179618-64-5 (4E,6E,10R)-10-methoxy-1-(4-methoxybenzyl)oxy-7-methyltrideca-4,6,12-triene 
• 179618-62-3 (4E,6E)-10-(4-Methoxy-benzyloxy)-4-methyl-deca-4,6-dienal 

Relevant articles and documents

Synthetic study on curacin A: A novel antimitotic agent from the cyanobacterium Lyngbya majuscula

Curacin A (1), a novel antimitotic agent, was synthesized in a highly stero-controlled manner. The four stereoisomers of a partial structure at the thiazoline moiety, 2 were also synthesized to aid in elucidation of the absolute configurations of three chiral centers in curacin A. The effects of porcine brain tubulin assembly of several synthetic compounds related to curacin A were examined.