36742-36-6

Basic information

• Product Name: 1-(cyclopent-1-en-1-yl)-3-methoxybenzene
• CAS NO: 36742-36-6
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.239
• Mol File: 36742-36-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 277.6°C at 760 mmHg
• Flash Point: 106.5°C
• Density: 1.035g/cm³
• Vapor Pressure: 0.00756mmHg at 25°C
• Refractive Index: 1.552
• CAS DataBase Reference: 1-(cyclopent-1-en-1-yl)-3-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(cyclopent-1-en-1-yl)-3-methoxybenzene(36742-36-6)
• EPA Substance Registry System: 1-(cyclopent-1-en-1-yl)-3-methoxybenzene(36742-36-6)

Safety Data

• Hazardous Substances Data: 36742-36-6(Hazardous Substances Data)

Usage

General Description

1-(cyclopent-1-en-1-yl)-3-methoxybenzene, also known as 1-(1-cyclopenten-1-yl)-3-methoxybenzene, is a chemical compound with the molecular formula C12H14O. It is a derivative of benzene with a cyclopentenyl group and a methoxy group attached to the benzene ring. 1-(cyclopent-1-en-1-yl)-3-methoxybenzene is commonly used in organic synthesis and pharmaceutical research. Its properties and potential uses are still being explored, and it may have applications in the development of new drugs and other industrial products. Additionally, its structure and reactivity make it an interesting target for further study in organic chemistry.

Upstream product

• 66107-33-3 3-methoxyphenyl triflate 
• 142-29-0 cyclopentene 
• 2398-37-0 3-methoxyphenyl bromide 
• 120-92-3 cyclopentanone 
• 142144-65-8 1-(3-methoxyphenyl) cyclopentan-1-ol 
• 36282-40-3 (3-methoxyphenyl)magnesium bromide 

Downstream Products

• 142144-66-9 3-cyclopent-1-enyl-phenol 
• 75146-71-3 1-(3-methoxyphenyl)-6-oxabicyclo[3.1.0]hexane 
• 64417-35-2 2-Brom-5-(N-Carbethoxy-N-methylaminoethyl)-5-(3-methoxyphenyl)-cyclopent-2-enon 
• 64417-33-0 2-(N-Carbethoxy-N-methylaminoethyl)-2-(3-methoxyphenyl)-cyclopentanon 
• 64417-34-1 5-(N-Carbethoxy-N-methylaminoethyl)-5-(3-methoxyphenyl)-cyclopent-2-enon 
• 342405-60-1 2-(3-Methoxyphenyl)-2-(2-dimethylaminoethyl)-cyclopentanon 
• 61321-35-5 2-(3-Dimethylaminopropyl)-2-(3-methoxyphenyl)cyclopentanon 
• 288591-15-1 {(2R,6S)-6-[3-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-tetrahydro-pyran-2-yl}-acetic acid methyl ester 
• 288591-14-0 (E)-(S)-7-[3-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-7-hydroxy-hept-2-enoic acid methyl ester 
• 288591-02-6 7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester 
• 288591-03-7 7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-hydroxy-hept-2-enoic acid methyl ester 
• 288591-01-5 5-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-5-oxo-pentanal 

Relevant articles and documents

Nickel-catalyzed Heck reaction of cycloalkenes using aryl sulfonates and pivalates

Nickel-catalyzed Heck reaction of cycloalkenes delivers unusual conjugated arylated isomers. Nickel(0) catalysts ligated by chelating dialkylphosphines effectively activate not only aryl triflates as electrophiles, but also less reactive aryl mesylates, t

Arenediazonium o-benzenedisulfonimides as efficient reagents for Heck-type arylation reactions

Arenediazonium o-benzenedisulfonimides can be used as new and efficient reagents for Heck-type arylation reactions of some common substrates containing C-C multiple bonds, namely ethyl acrylate, acrylic acid, acroleyne, styrene and cyclopentene. The reactions were carried out in an organic solvent, in the presence of Pd(OAc)2 as pre-catalyst, and gave rise to arylated products, for example, ethyl cinnamates, cinnamic acids, cinnamic aldehydes and stilbenes, possessing an (E)-configuration, and 1-arylcyclopentenes, in good to excellent yields. It is noteworthy that all the reactions led to the recovery, in greater than 80% yield, of o-benzenedisulfonimide, recyclable for the preparation of other diazonium salts.

Synthesis and pharmacological activity of 6-aryl-2-azabicyclo[4.2.1]nonanes

A series of 6-phenyl-, 6-(m-methoxyphenyl)- and 6-(m-hydroxyphenyl)-2-azabicylo[4.2.1]nonanes was synthesized by a sequence involving alkylation of an appropriate 2-arylcyclopentanone with an aminoalkyl substituent. Subsequent ring closure at the other α