39831-53-3

Basic information

• Product Name: Benzene, 1-(2-butenyl)-4-methoxy-
• CAS NO: 39831-53-3
• Molecular Formula: C11H14O
• Molecular Weight: 162.232
• Mol File: 39831-53-3.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(2-butenyl)-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(2-butenyl)-4-methoxy-(39831-53-3)
• EPA Substance Registry System: Benzene, 1-(2-butenyl)-4-methoxy-(39831-53-3)

Safety Data

• Hazardous Substances Data: 39831-53-3(Hazardous Substances Data)

Upstream product

• 6117-91-5 (E/Z)-2-buten-1-ol 
• 100-66-3 methoxybenzene 
• 1261958-96-6 1-(3-benzyloxybut-1-enyl)-4-methoxylbenzene 
• 689-89-4 (2E,4E)-methylhexa-2,4-dienoate 
• 140-67-0 Estragole 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 2516-33-8 Cyclopropylmethanol 
• 4894-61-5 trans-but-2-enyl chloride 
• 6737-11-7 2-acetoxy-3-butene 
• 106-99-0 buta-1,3-diene 
• 67952-38-9 4-(4-methoxy-phenyl)-butan-2-ol 
• 696-62-8 para-iodoanisole 
• 591-97-9 1-chloro-2-butene 
• 628-08-0 crotyl acetate 

Downstream Products

• 84736-54-9 2-(4-methoxyphenyl)-3-pentanone 
• 53917-01-4 1-(4-methoxyphenyl)butan-2-one 
• 18272-84-9 4-n-butylanisole 
• 857590-49-9 4-(1,2-dibromo-butyl)-anisole 
• 5789-34-4 meso-4,5-bis-(4-methoxy-phenyl)-octane 
• 5789-34-4 racem.-4,5-bis-(4-methoxy-phenyl)-octane 

Relevant articles and documents

Spicing up olefin cross metathesis with the renewables estragole and methyl sorbate

Diene moieties conjugated to a carbonyl group are ubiquitous in nature and are present in compounds with relevant biological properties. Herein we investigate the cross metathesis (CM) of the renewable cross partners estragole and methyl sorbate (MeSo) to produce methyl 6-(4-methoxyphenyl)hexa-2,4-dienoate. By the judicious choice of the ruthenium-based metathesis catalysts, as well as the reaction conditions, it was possible to obtain good conversion and selectivity for the desired product in catalyst loadings as low as 50 ppm (0.005 mol%), with a minimal amount of solvent.

Revisiting Allylic Coupling of Grignard Reagents: Nano Copper Catalyzed One-Pot α-Selective Aryl-Allyl Coupling

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Practical iron-catalyzed allylations of aryl grignard reagents

An operationally simple iron-catalyzed reductive cross-coupling reaction between aryl halides and allyl electrophiles has been developed. The underlying domino process exhibits high versatility with respect to the allylic leaving group (acetate, tosylate, diethyl phosphate, methyl carbonate, trimethylsilanolate, methanethiolate, chloride, bromide) and high economic and environmental sustainability with respect to the catalyst system (0.2-5 mol% tris(acetylacetonato)iron(III), ligand-free) and reaction conditions (tetrahydrofuran, 0°C, 45 min).