70214-59-4

Basic information

• Product Name: 4-Pentynal, 5-phenyl-
• CAS NO: 70214-59-4
• Molecular Formula: C11H10O
• Molecular Weight: 158.2
• Mol File: 70214-59-4.mol
• Article Data: 30

Chemical Properties

• CAS DataBase Reference: 4-Pentynal, 5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pentynal, 5-phenyl-(70214-59-4)
• EPA Substance Registry System: 4-Pentynal, 5-phenyl-(70214-59-4)

Safety Data

• Hazardous Substances Data: 70214-59-4(Hazardous Substances Data)

Upstream product

• 17733-79-8 (E)-5-phenyl-penta-2-ene-4-yne-1-ol 
• 30625-91-3 (E)-5-phenylpent-2-en-4-ynal 
• 27948-27-2 (E)-methyl 5-phenylpent-2-en-4-ynoate 
• 2579-22-8 Phenylpropargyl aldehyde 
• 108-86-1 bromobenzene 
• 1276664-59-5 (5,5-diethoxypent-1-yn-1-yl)benzene 
• 591-50-4 iodobenzene 
• 536-74-3 phenylacetylene 
• 4440-01-1 lithium phenylacetylide 
• 5390-04-5 pent-1-yn-5-ol 
• 2170-06-1 1-Phenyl-2-(trimethylsilyl)acetylene 
• 107-02-8 acrolein 
• 24595-58-2 5-phenylpent-4-yn-1-ol 

Downstream Products

• 130066-05-6 2-(1-Hydroxy-5-phenyl-pent-4-ynyl)-2-methyl-cyclohexanone 
• 130066-06-7 2-(1-Hydroxy-5-phenyl-pent-4-ynyl)-2-methyl-cycloheptanone 
• 130066-09-0 2-(1-Hydroxy-5-phenyl-pent-4-ynyl)-2-methyl-cyclopentanone 
• 92993-97-0 N-isobutyl-7-phenylhept-2E-en-6-ynamide 
• 92994-36-0 ethyl (2E)-7-phenylhept-2-en-6-ynoate 
• 24595-57-1 6-phenyl-5-hexyn-2-ol 
• 144269-92-1 1,7-diphenyl-3-hydroxy-1,6-heptadiyne 

Relevant articles and documents

Method for efficiently synthesizing 1,6-diene-3-ketone derivatives

The invention discloses a method for efficiently synthesizing 1,6-diene-3-ketone derivatives, which comprises the following steps: in an organic solvent system, taking a compound represented by a formula 2 as a raw material, carrying out stirring reflux r

Chemoselective Biohydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2-Alkynals/3-Alkyn-2-ones into 4-Alkynals/Alkynols

The chemoselective hydrogenation of alkenes in the presence of alkynes is a very challenging transformation to achieve with traditional chemical methods. The development of an effective procedure to perform this transformation would enrich the tool-kit available to organic chemists for the development of useful synthetic routes, and the creation of novel structural motifs. The reduction of activated alkene bonds by ene-reductases (ERs) is completely chemoselective, because of the mechanism of the reaction. Thus, we investigated the use of ERs belonging to the Old Yellow Enzyme family for the reduction of α,β-unsaturated aldehydes with a conjugated C≡C triple bond at the γ position. This reaction was exploited as the key step for the development of an effective homologation route to convert aryl and alkyl substituted propynals and butynones into 4-alkynals and 4-alkynols, avoiding some troublesome or hazardous steps of known synthetic routes. (Figure presented.).

Development of Hybrid Phospholipid Mimics as Effective Agonists for Liver Receptor Homologue-1

The orphan nuclear receptor Liver Receptor Homologue-1 (LRH-1) is an emerging drug target for metabolic disorders. The most effective known LRH-1 modulators are phospholipids or synthetic hexahydropentalene compounds. While both classes have micromolar ef