86838-43-9

Basic information

• Product Name: 6-Heptenal, 2-(phenylmethoxy)-, (2R)-
• CAS NO: 86838-43-9
• Molecular Formula: C14H18O2
• Molecular Weight: 218.296
• Mol File: 86838-43-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 6-Heptenal, 2-(phenylmethoxy)-, (2R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Heptenal, 2-(phenylmethoxy)-, (2R)-(86838-43-9)
• EPA Substance Registry System: 6-Heptenal, 2-(phenylmethoxy)-, (2R)-(86838-43-9)

Safety Data

• Hazardous Substances Data: 86838-43-9(Hazardous Substances Data)

Upstream product

• 86838-41-7 (4S,5S)-4-((R)-1-Benzyloxy-hex-5-enyl)-2,2,5-trimethyl-[1,3]dioxolane 
• 100-39-0 benzyl bromide 
• 874910-11-9 (4S,5S)-4,5-bis((R)-1-(benzyloxy)hex-5-enyl)-2,2-dimethyl-1,3-dioxolane 
• 874910-10-8 (4S,5S)-4,5-bis((R)-1-hydroxyhex-5-enyl)-2,2-dimethyl-1,3-dioxolane 
• 874910-09-5 (4R,5R)-4,5-bis(hex-5-enoyl)-2,2-dimethyl-1,3-dioxolane 
• 86838-42-8 (2S,3S,4R)-4-Benzyloxy-non-8-ene-2,3-diol 
• 1035798-17-4 1-(Tetrahydro-pyran-2-yloxy)-hept-6-en-2-ol 
• 132295-41-1 2-Benzyloxy-hept-6-en-1-ol 

Downstream Products

• 132198-28-8 4-Benzyloxy-non-8-en-3-ol 
• 86838-45-1 (R)-2-(benzyloxy)hept-6-en-1-ol 
• 132198-30-2 (3R,4R)-4-(benzyloxy)non-8-en-3-ol 
• 950826-37-6 (2R,3R)-3-(benzyloxy)oct-7-en-2-ol 
• 950826-40-1 (7R,8R)-7,8-bis(benzyloxy)nonan-3-ol 
• 950826-43-4 (7R,8R)-7,8-bis(benzyloxy)nonan-3-one 
• 80502-06-3 (6R,7R)-6-(benzyloxy)-7-hydroxynonan-2-one 
• 78843-64-8 (2R)-heptane-1,2-diol 
• 86838-50-8 ((S)-1-Pent-4-enyl-dodecyloxymethyl)-benzene 
• 86838-49-5 Toluene-4-sulfonic acid (R)-2-benzyloxy-hept-6-enyl ester 
• 132198-29-9 (3S,4R)-4-Benzyloxy-non-8-en-3-ol 
• 132295-42-2 4-Benzyloxy-non-8-en-3-one 
• 132198-26-6 (R)-4-benzyloxy-8-nonen-3-one 
• 80502-06-3 (6R,7S)-6-(benzyloxy)-7-hydroxynonan-2-one 

Relevant articles and documents

Enantioselective synthesis of α-benzyloxy-ω-alkenals: application to the synthesis of (+)-exo-brevicomin, (+)-iso-exo-brevicomin, and (-)-isolaurepan

The enantioselective synthesis of α-benzyloxy aldehydes containing a terminal alkene was carried out from chiral pool l-(+)-tartaric acid by employing the stereoselective reduction of a 1,4-diketone as the key step. The synthetic utility of these aldehyde

Synthesis of (+)-endo- and (+)-exo-brevicomin viaenzyme-mediated hydrolysis of an enol ester

Optically pure (+)-endo- and (+)-exo-brevicomin have been synthesized in short steps starting from α-hydroxy ketone derivative, (R)-4-benzyloxy-8-nonen-3-one (3), which was prepared via enzymatic hydrolysis of racemic enol ester 4.