117661-29-7

Basic information

• Product Name: 1-Penten-3-ol, 5-(phenylmethoxy)-
• CAS NO: 117661-29-7
• Molecular Formula: C12H16O2
• Molecular Weight: 192.258
• Mol File: 117661-29-7.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: 1-Penten-3-ol, 5-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Penten-3-ol, 5-(phenylmethoxy)-(117661-29-7)
• EPA Substance Registry System: 1-Penten-3-ol, 5-(phenylmethoxy)-(117661-29-7)

Safety Data

• Hazardous Substances Data: 117661-29-7(Hazardous Substances Data)

Upstream product

• 19790-60-4 3-Benzyloxypropanal 
• 1826-67-1 vinyl magnesium bromide 
• 90246-36-9 5-(benzyloxy)-1-pentyn-3-ol 
• 4799-68-2 3-benzyloxypropan-1-ol 
• 85960-55-0 (S)-(2-phenylmethoxyethyl)oxirane 
• 100-44-7 benzyl chloride 
• 115114-87-9 (2R)-2-(2-benzyloxyethyl)oxirane 
• 1013651-95-0 (2R,3S)-2-(2-benzyloxy-ethyl)-3-(iodomethyl)oxirane 
• 119180-88-0 (E)-(R)-5-Benzyloxy-1-trimethylsilanyl-pent-1-en-3-ol 
• 119046-50-3 (E)-5-Benzyloxy-1-trimethylsilanyl-pent-1-en-3-ol 
• 88191-39-3 (Z)-((hex-3-en-1-yloxy)-methyl)benzene 
• 100-39-0 benzyl bromide 
• 5470-84-8 4-benzyloxybutanal 
• 4541-14-4 4-benzyloxy-butan-1-ol 

Downstream Products

• 320749-20-0 5-(benzyloxy)pent-1-en-3-one 
• 176848-41-2 1-phenylmethoxy-3-pentanone 
• 184343-66-6 4-(2-benzyloxyethyl)-1,3-dioxan-2-one 
• 1013651-96-1 1-(((R)-3-(2-bromo-1-ethoxyethoxy)-pent-4-enyloxy)methyl)benzene 
• 1240372-16-0 C₂₈H₃₄O₂Si 
• 1404461-23-9 C₁₉H₂₁F₂NO 
• 1404461-11-5 C₁₄H₁₆Cl₃NO₂ 

Relevant articles and documents

A highly stereoselective synthesis of Z-disubstituted olefin by O-assisted Still-Wittig rearrangement

In the Still-Wittig rearrangement, stannylated methyl (E)-allylic ethers having an aliphatic side chain (1a-c) exhibited the usual similar stereoselectivity, although the poor stereoselectivity was remarkably improved by the assistance of an alkoxy moiety on the alkenyl chain. A stannylated methyl (Z)-allylic ether bearing an alkoxy moiety on the alkenyl chain (1e) also showed a high E selectivity as previously reported.

Visible-Light Photoredox-Catalyzed α-Regioselective Conjugate Addition of Allyl Groups to Activated Alkenes

The α-regioselective conjugate addition of allyl groups to activated alkenes is a poorly explored area of research. Herein, we report an α-adduct and (E)-isomer selective conjugate addition of allylsilanes to activated alkenes by visible-light photoredox catalysis. The reaction involves allylic radicals that can be generated from allylsilanes through a photoinduced single-electron transfer mechanism. (Figure presented.).

C-20 STEROID COMPOUNDS, COMPOSITIONS AND USES THEREOF TO TREAT TRAUMATIC BRAIN INJURY (TBI), INCLUDING CONCUSSIONS

The present invention relates to C-20 steroid compounds, compositions and methods of use thereof to treat, minimize and/or prevent traumatic brain injury (TBI), including severe TBI, moderate TBI and mild TBI, including concussions.