90865-70-6

Basic information

• Product Name: Butanal, 3-methyl-4-(phenylmethoxy)-, (3R)-
• CAS NO: 90865-70-6
• Molecular Formula: C12H16O2
• Molecular Weight: 192.258
• Mol File: 90865-70-6.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Butanal, 3-methyl-4-(phenylmethoxy)-, (3R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanal, 3-methyl-4-(phenylmethoxy)-, (3R)-(90865-70-6)
• EPA Substance Registry System: Butanal, 3-methyl-4-(phenylmethoxy)-, (3R)-(90865-70-6)

Safety Data

• Hazardous Substances Data: 90865-70-6(Hazardous Substances Data)

Upstream product

• 63930-49-4 (R)-3-(benzyloxy)-2-methylpropan-1-ol 
• 126788-88-3 (R)-1-((2-methylpent-4-enyloxy)methyl)benzene 
• 126788-89-4 (R)-5-Benzyloxy-1-hydroxy-4-methyl-pentan-2-one 
• 90809-13-5 (E)-4-(Benzyloxy)-N,N-diethyl-3-methylbut-2-enylamine 
• 90809-26-0 1-<(1E,3R)-4-(Benzyloxy)-3-methylbut-1-enyl>piperidine 
• 90809-27-1 4-<(1E,3R)-4-(Benzyloxy)-3-methylbut-1-enyl>morpholine 
• 90809-25-9 (1E,3R)-4-(Benzyloxy)-N,N-dibutyl-3-methylbut-1-enylamine 
• 91458-94-5 (1E,3R)-4-(Benzyloxy)-N,N-diethyl-3-methylbut-1-enylamine 
• 156625-00-2 ((E)-(R)-2-Methyl-hex-4-enyloxymethyl)-benzene 
• 104265-24-9 (3R)-4-benzyloxy-3-methyl-butanonitrile 
• 128693-46-9 Methanesulfonic acid (S)-3-benzyloxy-2-methyl-propyl ester 
• 63501-27-9 (2R)-2-methyl-4-penten-1-ol 
• 116996-56-6 (4S)-4-benzyl-3-[(2R)-2-methylpent-4-enoyl]oxazolidin-2-one 
• 100-39-0 benzyl bromide 

Downstream Products

• 174172-43-1 (3R,4S)-5-Benzyloxy-2,2-difluoro-3-hydroxy-4-methyl-pentanoic acid ethyl ester 
• 126788-91-8 (4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one 
• 156625-01-3 (4R,5S)-3-((2R,3S,5R)-2,6-Bis-benzyloxy-3-hydroxy-5-methyl-hexanoyl)-4-methyl-5-phenyl-oxazolidin-2-one 
• 73408-07-8 (R)-4-(Benzyloxy)-3-methylbutan-1-ol 
• 128693-47-0 (R)-4-(Benzyloxy)-3-methylbutanoic acid 
• 273733-89-4 (4S,6R)-7-(benzyloxy)-6-methylhept-1-en-4-ol 
• 273733-90-7 (2R,4S)-1-benzyloxy-2-methyl-6-hepten-4-yl-propenoate 
• 945908-20-3 C₁₉H₃₄O₂Si 
• 945908-23-6 C₅₀H₉₆O₈Si₃ 
• 945908-27-0 C₅₀H₉₄O₈Si₃ 
• 394657-32-0 [(2R,4S)-4-(1-Ethoxy-allyloxy)-2-methyl-hept-6-enyloxymethyl]-benzene 
• 115268-43-4 laulimalide 
• 273733-91-8 (S)-6-((R)-3-(benzyloxy)-2-methylpropyl)-5,6-dihydro-2H-pyran-2-one 
• 1027233-25-5 Acetic acid (S)-6-((R)-3-benzyloxy-2-methyl-propyl)-5,6-dihydro-2H-pyran-2-yl ester 

Relevant articles and documents

SUBSTITUTED PYRAZOLOAZEPIN-8-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS

The present invention relates to novel pyrazoloazepin-8-ones with phosphodiesterase inhibitory activity, as well as to their use as therapeutic agents in the treatment of inflammatory diseases and conditions.

Synthesis of optically active β- Or γ-alkyl-substituted alcohols through copper-catalyzed asymmetric allylic alkylation with organolithium reagents

An efficient one-pot synthesis of optically active β-alkyl-substituted alcohols through a tandem copper-catalyzed asymmetric allylic alkylation (AAA) with organolithium reagents and reductive ozonolysis is presented. Furthermore, hydroboration-oxidation following the Cu-catalyzed AAA leads to the corresponding homochiral γ-alkyl-substituted alcohols.

Hydride reduction of alpha, beta-unsaturated carbonyl compounds using chiral organic catalysts

Nonmetallic, chiral organic catalysts are used to catalyze the 1,4-hydride reduction of an α,β-unsaturated carbonyl compound. The α,β-unsaturated carbonyl compound may be an aldehyde or cyclic ketone, and the hydride donor may be a dihydropyridine. The reaction is enantioselective, and proceeds with a variety of hydride donors, catalysts, and substrates. The invention also provides compositions effective in carrying out the 1,4-hydride addition of α,β-unsaturated carbonyl compounds.