119649-45-5

Basic information

• Product Name: 1-Butanol, 4-[(4-methoxyphenyl)methoxy]-
• CAS NO: 119649-45-5
• Molecular Formula: C12H18O3
• Molecular Weight: 210.273
• Mol File: 119649-45-5.mol
• Article Data: 56

Chemical Properties

• CAS DataBase Reference: 1-Butanol, 4-[(4-methoxyphenyl)methoxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanol, 4-[(4-methoxyphenyl)methoxy]-(119649-45-5)
• EPA Substance Registry System: 1-Butanol, 4-[(4-methoxyphenyl)methoxy]-(119649-45-5)

Safety Data

• Hazardous Substances Data: 119649-45-5(Hazardous Substances Data)

Usage

Description

1-Butanol, 4-[(4-methoxyphenyl)methoxy]-, also known as p-anisyl butyl ether, is a chemical compound that features a butanol molecule with a 4-(4-methoxyphenyl)methoxy group attached to it. It is a clear, colorless liquid with a mild, sweet odor and is slightly soluble in water.
Used in Food Industry:
1-Butanol, 4-[(4-methoxyphenyl)methoxy]is used as a flavoring agent for its mild, sweet odor, enhancing the taste and aroma of various food products.
Used in Perfume Industry:
1-Butanol, 4-[(4-methoxyphenyl)methoxy]is used as a fragrance ingredient in perfumes, contributing to the creation of unique and pleasant scents.
Used in Pharmaceutical Industry:
1-Butanol, 4-[(4-methoxyphenyl)methoxy]is used in the production of pharmaceuticals, potentially serving as a solvent or a component in the formulation of medications.
Used in Solvent Production:
1-Butanol, 4-[(4-methoxyphenyl)methoxy]is used in the production of solvents, which are essential in various industrial processes and applications.
Used in Biofuel Research:
1-Butanol, 4-[(4-methoxyphenyl)methoxy]has been studied for its potential use as a biofuel, offering an alternative, renewable energy source.
It is important to handle 1-Butanol, 4-[(4-methoxyphenyl)methoxy]with care, as it can be harmful if ingested, inhaled, or absorbed through the skin.

Upstream product

• 110-63-4 Butane-1,4-diol 
• 824-94-2 p-methoxybenzyl chloride 
• 1082056-33-4 Bis(4-methoxyphenyl)methyl 4-methoxybenzyloxybutyl ether 
• 105-13-5 4-Methoxybenzyl alcohol 
• 100-07-2 4-methoxy-benzoyl chloride 
• 431065-45-1 1-methoxy-4-{[4-(trityloxy)butoxy]methyl}benzene 
• 2746-25-0 p-Methoxybenzyl bromide 
• 27063-62-3 2-(4-methoxy-phenyl)-[1,3]dioxepane 

Downstream Products

• 154476-70-7 6-(4-methoxybenzyloxy)hex-1-en-3-ol 
• 442156-77-6 4-(tert-butyldiphenylsilanyloxy)-1-(4-methoxybenzyloxy)-5-hexene 
• 1082056-33-4 Bis(4-methoxyphenyl)methyl 4-methoxybenzyloxybutyl ether 
• 1586033-64-8 (S,Z)-1-((4S,5S)-5-((R)-1-(tert-butyldiphenylsilyloxy)octyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-(4-methoxybenzyloxy)hex-1-en-3-ol 
• 1586033-54-6 tert-butyl((R)-1-((4S,5S)-5-((S,E)-6-(4-methoxybenzyloxy)-3-(methoxymethoxy)hex-1-enyl)-2,2-dimethyl-1,3-dioxolan-4-yl)octyloxy)diphenylsilane 
• 1586033-62-6 tert-butyl-((R)-1-((4S,5S)-5-((S,Z)-6-(4-methoxybenzyloxy)-3-(methoxymethoxy)hex-1-enyl)-2,2-dimethyl-1,3-dioxolan-4-yl)octyloxy)diphenylsilane 
• 1586033-45-5 (S)-6-(4-methoxybenzyloxy)hex-1-en-3-yl acetate 
• 1571059-44-3 (S)-6-(4-methoxybenzyloxy)hex-1-en-3-ol 
• 1586033-46-6 (S)-1-methoxy-4-((4-(methoxymethoxy)hex-5-enyloxy)methyl)benzene 
• 1586033-53-5 (S,E)-1-((4S,5S)-5-((R)-1-(tert-butyldiphenylsilyloxy)octyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-(4-methoxybenzyloxy)hex-1-en-3-ol 
• 286440-96-8 1-[(4-bromobutoxy)methyl]-4-methoxy benzene 
• 164933-38-4 1-{[(4-iodobutyl)oxy]methyl}-4-methoxybenzene 
• 431065-45-1 1-methoxy-4-{[4-(trityloxy)butoxy]methyl}benzene 
• 643016-64-2 (R)-tert-butyl((6-((4-methoxybenzyl)oxy)hexan-2-yl)oxy)dimethylsilane 

Relevant articles and documents

The di-t-butylsilylene protecting group as a bridging unit in linear and macrocyclic bis-malonates for the regioselective multifunctionalization of C60

Fullerene equatorial bis-adducts have been prepared with high regioselectivity by a double Bingel reaction between [60]fullerene and di-t-butylsilylene-tethered bis-malonates. Macrocyclic bis-malonates incorporating di-t-butylsilylene moieties have also b

Synthesis of Aminoallenes via Selenium-π-Acid-Catalyzed Cross-Coupling of N-Fluorinated Sulfonimides with Simple Alkynes

The facile synthesis of aminoallenes, accomplished by a selenium-π-acid-catalyzed cross-coupling of an N-fluorinated sulfonimide with simple, non-activated alkynes, is reported. Until now, aminoallenes were difficult to be accessed by customary means, inasmuch as pre-activated and, in part, intricate starting materials were necessary for their synthesis. In sharp contrast, the current study shows that ordinary internal alkynes can serve as simple and readily available precursors for the construction of the aminoallene motif. The operating reaction conditions tolerate numerous functional groups such as esters, nitriles, (silyl)ethers, acetals, and halogen substituents, furnishing the target compounds in up to 86 % yield.

Fluorine in pheromones: Synthesis of fluorinated 12-dodecanolides as emerald ash borer pheromone mimetics

A series of five 12-dodecanolides have been synthesised containing CF2 groups at C5, C6, C7, C8 and in one case, a double substitution at C5 & C8, as a strategy to bias the conformational space accessed by these macrocycles, and to assess if th