99902-35-9

Basic information

• Product Name: (R)-3-hydroxy-5-phenyl-1-pentyne
• Synonyms: (R)-3-hydroxy-5-phenyl-1-pentyne;(R)-5-phenyl-1-pentyn-3-ol
• CAS NO: 99902-35-9
• Molecular Weight: 160.216
• EINECS: -0
• Mol File: 99902-35-9.mol
• Article Data: 57

Chemical Properties

• CAS DataBase Reference: (R)-3-hydroxy-5-phenyl-1-pentyne(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-hydroxy-5-phenyl-1-pentyne(99902-35-9)
• EPA Substance Registry System: (R)-3-hydroxy-5-phenyl-1-pentyne(99902-35-9)

Safety Data

• Hazardous Substances Data: 99902-35-9(Hazardous Substances Data)

Usage

General Description

(R)-3-hydroxy-5-phenyl-1-pentyne is a chemical compound with the molecular formula C11H12O. It is an alkyne compound with a hydroxyl group and a phenyl group attached to a pentynyl chain. (R)-3-hydroxy-5-phenyl-1-pentyne is a chiral molecule, with the (R) configuration indicating the arrangement of substituent groups around the stereocenter. (R)-3-hydroxy-5-phenyl-1-pentyne has potential applications in organic synthesis, as well as in the pharmaceutical and chemical industries. It may also be of interest in research related to the properties and reactivity of alkynes and chiral compounds.

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 1066-26-8 sodium acetylide 
• 65032-27-1 ethynylmagnesium chloride 
• 1027627-26-4 C₂₀H₃₄OSi₂ 
• 110211-31-9 Acetic acid 1-phenethyl-3-trimethylsilanyl-prop-2-ynyl ester 
• 67-56-1 methanol 
• 100330-45-8 (+/-)-1-(2-Phenylethyl)-3-propynyl acetate 
• 108-05-4 vinyl acetate 
• 99902-35-9 5-phenylpent-1-yn-3-ol 
• 118584-91-1 5-phenylpent-1-yn-3-one 
• 99902-30-4 (3R,5R)-3-methyl-5-(2'-phenylethyl)-4-oxahept-6-insaeure 
• 591-50-4 iodobenzene 
• 621-82-9 Cinnamic acid 
• 122-97-4 3-Phenyl-1-propanol 

Downstream Products

• 130325-03-0 (Z)-(S)-1-Iodo-5-phenyl-pent-1-en-3-ol 
• 453574-71-5 3,3-dimethyl-5-phenylethyl-4-oxa-3-sila-1-hepten-6-yne 
• 710313-46-5 (E)-6-methyl-1-phenyloct-6-en-4-yn-3-ol 
• 919284-01-8 (R)-5-phenylpent-1-yn-3-yl propionate 
• 913977-01-2 C₁₅H₁₈O 
• 135450-17-8 6-methylene-5-(2-phenylethyl)-1,4-dioxan-2-one 
• 135450-12-3 (1-ethynyl-3-phenylpropoxy)acetic acid 
• 1155369-75-7 C₁₈H₁₉N₃O 
• 1190883-31-8 C₁₂H₁₂O₂ 
• 183904-28-1 (S)-5-phenyl-1-pentyn-3-ol 
• 4024-14-0 1-methyl-2-tetralone 
• 1347047-35-1 (3-fluoropent-4-en-1-yl)benzene 

Relevant articles and documents

Sc(OTf)3-catalyzed [3 + 2]-cycloaddition of nitrones with ynones

An efficient approach to access functionalized (2,3-dihydroisoxazol-4-yl) ketones has been developed by reacting nitrones 4 with ynones 7 or terminal ynones 10 in a one-pot fashion. The reaction went through a formal Sc(OTf)3-catalyzed [3 + 2]-cycloaddition process to generate a number of functionalized (2,3-dihydroisoxazol-4-yl) ketones 11aa-11aw, 11ba-11la and 12aa-12ae in moderate to good yields. This journal is

Synthesis of Difluorinated Dihydrobenzo[de]chromenes via Rh(III)-Catalysed C-H Couplings of 1-Naphthols with Gem-Difluoromethylene Alkynes

The Rh(III)-catalysed C?H couplings of 1-naphthols with gem-difluoromethylene alkynes have been realized for the direct construction of difluorinated dihydrobenzo[de]chromenes with broad substrate/functional group compatibility and good regio-/chemoselect

Transition-Metal-Free Synthesis of Electron Rich 1,3-Dienes via Base Promoted Isomerization of Propargylic Ethers

Herein, a novel and scalable synthesis of electron rich 1,3-dienes based on KOtBu mediated isomerization of propargylic ether derivatives was developed. This new process features easy handling reaction conditions, transition-metal-free isomerization, high isolated yields, and most of all, it could be used for modification of natural products at late stage functionalizations.