7380-78-1

Basic information

• Product Name: 1-METHOXY-4-PHENYLETHYNYL-BENZENE
• Synonyms: 1-METHOXY-4-PHENYLETHYNYL-BENZENE;(p-Anisylethynyl)benzene;1-(Phenylethynyl)-4-methoxybenzene;2-(4-Methoxyphenyl)-1-phenylethyne;4-(Phenylethynyl)anisole;4-Methoxy-1-(phenylethynyl)benzene;Benzene, 1-Methoxy-4-(phenylethynyl)-;1-[2-(4-Methoxyphenyl)ethynyl]benzene
• CAS NO: 7380-78-1
• Molecular Formula: C₁₅H₁₂O
• Molecular Weight: 208.25518
• Mol File: 7380-78-1.mol
• Article Data: 475

Chemical Properties

• Melting Point: 95℃
• Boiling Point: 339.007 °C at 760 mmHg
• Flash Point: 155.389 °C
• Appearance: /
• Density: 1.103 g/cm³
• CAS DataBase Reference: 1-METHOXY-4-PHENYLETHYNYL-BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-METHOXY-4-PHENYLETHYNYL-BENZENE(7380-78-1)
• EPA Substance Registry System: 1-METHOXY-4-PHENYLETHYNYL-BENZENE(7380-78-1)

Safety Data

• Hazardous Substances Data: 7380-78-1(Hazardous Substances Data)

Usage

General Description

1-METHOXY-4-PHENYLETHYNYL-BENZENE, also known as Anethole, is an organic compound commonly found in essential oils such as anise, fennel, and star anise. It possesses a sweet, aromatic scent and is often used as a flavoring agent in food and beverages. Anethole has been studied for its potential therapeutic properties, including anti-inflammatory and antioxidant effects. However, it is important to note that excessive consumption of anethole may have adverse health effects, so it is typically used in small quantities in commercial products. Overall, 1-METHOXY-4-PHENYLETHYNYL-BENZENE plays a significant role in the flavoring and fragrance industries and has potential medicinal applications.

Upstream product

• 611-94-9 4-Methoxybenzophenone 
• 25411-73-8 diethyl diazomethylphosphonate 
• 60059-95-2 C₉H₇ClF₂O 
• 591-51-5 phenyllithium 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 536-74-3 phenylacetylene 
• 696-62-8 para-iodoanisole 
• 3757-88-8 tributylstannylethynylbenzene 
• 3989-14-8 (4-methoxyphenylethynyl)trimethylsilane 
• 108-90-7 chlorobenzene 
• 26624-19-1 (α,α'-dibromo-bibenzyl-4-yl)-methyl ether 
• 71-36-3 butan-1-ol 
• 70744-47-7 (p-methoxyphenyl)tri-n-butylstannane 
• 768-60-5 4-methoxyphenylacetylen 

Downstream Products

• 94302-80-4 2-Phenyl-3-(4-methoxy-phenyl)-cyclopropen-⁽²⁾-carbonsaeure-⁽¹⁾-aethylester 
• 18648-74-3 2,2-diphenyl-1-(4-methoxyphenyl)ethylene 
• 1233-23-4 (Z)-1-(4-methoxyphenyl)-1,2-diphenylethylene 
• 134038-97-4 trans 1,4-bis (4-methoxyphenyl)-2,3-diphenyl-2-butene-1,4-dione 
• 1657-53-0 cis-4-methoxystilbene 
• 14310-21-5 1-(4-methoxyphenyl)-2-phenylethane 
• 846541-57-9 3t-(4-methoxy-phenyl)-2,3c-diphenyl-acrylic acid 

Relevant articles and documents

Synthesis and Optoelectronic Properties of Hexa-peri-hexabenzoborazinocoronene

The first rational synthesis of a BN-doped coronene derivative in which the central benzene ring has been replaced by a borazine core is described. This includes six C?C ring-closure steps that, through intramolecular Friedel–Crafts-type reactions, allow

Synthesis of Unprotected and Highly Substituted Indoles by the Ruthenium(II)-Catalyzed Reaction of Phenyl Isocyanates with Diaryl/Diheteroaryl Alkynes/Ethyl-3-phenyl Propiolates

A one-pot transformation has been developed for the synthesis of unprotected and highly substituted indoles by an in situ installed carbamide-directed Ru(II)-catalyzed intermolecular oxidative annulation of phenyl isocyanates with diaryl/diheteroaryl alkynes/ethyl phenyl propiolates in the presence of Cu(OAc)2·H2O as an oxidant and AgSbF6 as an additive at 120 °C within 3 h.

Introduction of a Recyclable Basic Ionic Solvent with Bis-(NHC) Ligand Property and The Possibility of Immobilization on Magnetite for Ligand- and Base-Free Pd-Catalyzed Heck, Suzuki and Sonogashira Cross-Coupling Reactions in Water

A new versatile and recyclable NHC ligand precursor has been developed with ligand, base, and solvent functionalities for the efficient Pd-catalyzed Heck, Suzuki and Sonogashira cross-coupling reactions under mild conditions. Furthermore, NHC ligand precursor was immobilized on magnetite and its catalytic activity was also evaluated towards the coupling reactions as a heterogeneous catalyst. The NHC ligand precursor was prepared with imidazolium functionalization of TCT followed by a simple ion exchange by hydroxide ions. However, the results revealed an excellent catalytic activity for the both homogeneous and heterogeneous catalytic systems. 1.52?g.cm?3 and 1194 cP was obtained for the density and viscosity of the NHC ligand precursor respectively. On the other hand, the heterogeneous type could be readily recovered from the reaction mixture and reused for several times while preserving its properties. Heterogeneous nature of the magnetic catalyst was studied by hot filtration, mercury poisoning, and three-phase tests. High to excellent yields were obtained for all entries for the both homogeneous and heterogeneous catalysts, which reflects the high consistency of the catalyst. Graphic Abstract: [Figure not available: see fulltext.]