916240-59-0

Basic information

• Product Name: Benzene, 1-methoxy-4-[[[(1R,2S)-2-methyl-1-[(1S)-1-methyl-2-(phenylmethoxy)eth yl]-4-penten-1-yl]oxy]methyl]-
• CAS NO: 916240-59-0
• Molecular Formula: C24H32O3
• Molecular Weight: 368.516
• Mol File: 916240-59-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methoxy-4-[[[(1R,2S)-2-methyl-1-[(1S)-1-methyl-2-(phenylmethoxy)eth yl]-4-penten-1-yl]oxy]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methoxy-4-[[[(1R,2S)-2-methyl-1-[(1S)-1-methyl-2-(phenylmethoxy)eth yl]-4-penten-1-yl]oxy]methyl]-(916240-59-0)
• EPA Substance Registry System: Benzene, 1-methoxy-4-[[[(1R,2S)-2-methyl-1-[(1S)-1-methyl-2-(phenylmethoxy)eth yl]-4-penten-1-yl]oxy]methyl]-(916240-59-0)

Safety Data

• Hazardous Substances Data: 916240-59-0(Hazardous Substances Data)

Upstream product

• 916240-61-4 (3S,4R,5S)-6-Benzyloxy-4-(4-methoxy-benzyloxy)-3,5-dimethyl-hexanal 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 916240-65-8 (4S,5S)-4-((S)-2-Benzyloxy-1-methyl-ethyl)-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxane 
• 63930-49-4 (R)-3-(benzyloxy)-2-methylpropan-1-ol 
• 79027-28-4 (2S)-3-(benzyloxy)-2-methylpropanal 
• 108393-28-8 (2S,3R,4S)-5-benzyloxy-2,3-dimethylpentane-1,4-diol 
• 167961-27-5 (2S,3R,4S)-5-Benzyloxy-3-(4-methoxy-benzyloxy)-2,4-dimethyl-pentan-1-ol 
• 183506-80-1 (4R,2'R,3'S,4'S)-4-benzyl-3-(5'-benzyloxy-3'-hydroxy-2',4'-dimethylpentanoyl)-2-oxazolidinone 
• 373645-80-8 (2R,3S,4S)-5-Benzyloxy-3-(4-methoxy-benzyloxy)-2,4-dimethyl-pentanal 

Downstream Products

• 916240-58-9 1-[(E)-(1R,2S,7R,8S,9S,10S)-1-((S)-2-Benzyloxy-1-methyl-ethyl)-7,9,11-tris-(tert-butyl-dimethyl-silanyloxy)-2,8,10-trimethyl-undec-4-enyloxymethyl]-4-methoxy-benzene 

Relevant articles and documents

A cross metathesis approach to the synthesis of the C11-C23 fragment of (-)-16-normethyldictyostatin

The synthesis of the C11-C23 fragment 2 of (-)-16-normethyldictyostatin has been achieved by cross metathesis between two olefinic fragments 4 and 5 followed by a reduction of the double bond at C16-C17. Both the olefinic fragments are easily synthesized