6712-31-8

Basic information

• Product Name: (-)-(R)-3-phenylpent-1-yn-3-ol
• CAS NO: 6712-31-8
• Molecular Weight: 160.216
• Mol File: 6712-31-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (-)-(R)-3-phenylpent-1-yn-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(R)-3-phenylpent-1-yn-3-ol(6712-31-8)
• EPA Substance Registry System: (-)-(R)-3-phenylpent-1-yn-3-ol(6712-31-8)

Safety Data

• Hazardous Substances Data: 6712-31-8(Hazardous Substances Data)

Upstream product

• 1066-26-8 sodium acetylide 
• 93-55-0 1-phenyl-propan-1-one 
• 74-86-2 acetylene 
• 1216963-74-4 lithium acetylide-ethylenediamine complex 
• 142034-43-3 3-phenylpent-1-yn-3-yl acetate 
• 88445-06-1 3-phenyl-1-pentyn-3-ol 
• 54655-07-1 lithium trimethylsilylacetylenide 

Downstream Products

• 88445-07-2 (R)-3-Phenyl-pent-1-yn-3-ol 
• 6712-31-8 (-)-(R)-3-phenylpent-1-yn-3-ol 
• 1169858-80-3 trimethyl(3-phenylpent-1-yn-3-yloxy)silane 
• 1366542-76-8 allyl (3-phenylpent-1-yn-3-yl) carbonate 
• 1383678-45-2 1-d-3-phenylpent-1-yn-3-ol 
• 1383678-42-9 1-d-3-phenylpent-1-yn-3-yl acetate 
• 93-55-0 1-phenyl-propan-1-one 
• 67231-20-3 (Z)-3-phenylpent-2-enenitrile 
• 65305-49-9 (E)-3-phenylpent-2-enenitrile 
• 1416772-16-1 ((3E,5E,7E)-4,7-dibromodeca-3,5,7-triene-3,8-diyl)dibenzene 
• 1203671-54-8 C₃₅H₄₇N₇OSi 
• 1203671-53-7 C₃₄H₄₄N₄O₂Si 
• 1203670-94-3 1-{2-amino-6-[5-(1-isopropyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]pyrimidin-4-yl}-1-phenylpropan-1-ol 
• 1203671-52-6 C₂₀H₃₂OSi 

Relevant articles and documents

Transition-Metal-Free Radical Hydrotrifluoromethylation of Alkynes

A combination of readily available and bench-stable CF3SO2Na and tBuOOH was efficiently used for hydrotrifluoromethylation of alkynes. An excellent trans-selectivity was demonstrated in the synthesis of alkenes. The developed mild reaction conditions allow the supression of the competing Meyer–Schuster-type rearrangement.

Allenyl ester precursors for 1H-inden-1-ol carboxylates: Comparisons with their propargylic equivalents having terminal alkyne functions

The reactivity of allenyl carboxylates, Ar(R1)CCCH(O 2CR2) and their isomeric equivalents the terminal propargylic carboxylates, ArC(R1)(O2CR2)CCH, in gold-catalyzed carbocyclization to ind

Hydrolytic Resolution of Tertiary Acetylenic Acetate Esters With the Lipase from Candida Cylindracea

The kinetic resolution of a series of tertiary acetylenic acetate esters using the lipase from Candida cylindracea has been explored.Compounds 6c and the trifluoromethyl acetate 6e have been resolved with high enantiomeric enrichment.Several other tertiary acetate esters carrying a CF3 group have been investigated which proved inert to enzymatic hydrolysis.From these results and published data, we are able to propose a predictive model for identifying the preferred enantiomer of secondary and tertiary trifluoromethyl acetate esters for this lipase.