5533-05-1

Usage

Uses

Used in Fragrance and Flavor Industry:
(2-methoxymethoxyphenyl)methanol is used as a fragrance and flavor compound for its pleasant scent, which is commonly added to perfumes, cosmetics, and personal care items.
Used in Pharmaceutical Industry:
(2-methoxymethoxyphenyl)methanol is used as a building block in organic synthesis for the manufacturing of pharmaceuticals, due to its versatility and stability.
Used in Consumer Products Industry:
(2-methoxymethoxyphenyl)methanol is used as an ingredient in various consumer products for its ability to impart a pleasant scent and its low toxicity, making it a safe and reliable component.

Upstream product

• 5533-04-0 2-(methoxymethoxy)benzaldehyde 
• 89-95-2 2-methyl-benzyl alcohol 
• 27701-23-1 methyl 2-(methoxymethyloxy)benzoate 
• 119-36-8 methyl salicylate 
• 69-72-7 salicylic acid 
• 90-02-8 salicylaldehyde 
• 824-91-9 O-methoxymethylphenol 

Downstream Products

• 73406-54-9 (2-Methoxymethoxyphenyl)methyl-methansulfonat 
• 4737-26-2 Isoflavan 
• 13524-66-8 2-benzyldihydrobenzofuran 
• 100976-02-1 2-phenyl-3-(2-hydroxyphenyl)-1-propanol 
• 152955-21-0 3-(2-O-methoxymethylphenyl)-2-phenyl-1-propanol 
• 152955-27-6 3-(2-Hydroxyphenyl)-2-(4-methoxyphenyl)-1-propanol 
• 152955-26-5 3-(2-hydroxyphenyl)-2-(2-methoxyphenyl)-1-propanol 
• 152955-16-3 methyl 3-(2-O-methoxymethylphenyl)-2-phenylpropanoate 
• 152955-23-2 2-(4-methoxyphenyl)-3-(2-O-methoxymethylphenyl)-1-propanol 
• 152955-22-1 2-(2-methoxyphenyl)-3-(2-O-methoxymethylphenyl)-1-propanol 
• 152955-18-5 methyl 2-(4-methoxyphenyl)-3-(2-O-methoxymethylphenyl)propanoate 
• 152955-17-4 methyl 2-(2-methoxyphenyl)-3-(2-O-methoxymethylphenyl)propanoate 
• 213970-54-8 1-(4-bromobenzenesulfonyloxy)-3-(2-hydroxyphenyl)-2-(4-methoxyphenyl)propane 
• 213970-39-9 3-(2-hydroxyphenyl)-2-(3,4-dimethoxyphenyl)-1-propanol 

Relevant academic research and scientific papers

Regioselective Fluorination of Acenes: Tailoring of Molecular Electronic Levels and Solid-State Properties

Optoelectronic properties of molecular solids are important for organic electronic devices and are largely determined by the adopted molecular packing motifs. In this study, we analyzed such structure-property relationships for the partially regioselectiv

Cationic Alkynyl Heck Reaction toward Substituted Allenes Using BobCat: A New Hybrid Pd(0)-Catalyst Incorporating a Water-Soluble dba Ligand

The cationic alkynyl Heck reaction between aryl triflates and alkynes to give substituted allenes is described. Key to the success of this method was the discovery and development of a new hybrid Pd(0)-catalyst, BobCat, that incorporates a water-soluble dba-ligand and biaryl phosphine ligand to provide substituted allenes in good yields under mild reaction conditions.

BITTER TASTE MODULATORS

The present invention includes antagonists of human type 2 taste receptors (hT2Rs) having structural Formula (I). The present invention also provides compositions containing these antagonists, the use of these antagonists for modulating taste perception, particularly bitter taste, and the method of preparing these antagonists (I).

Pt(IV)-catalyzed generation and [4+2]-cycloaddition reactions of o-quinone methides

Novel intermolecular and intramolecular generations of ortho-quinone methides and their formal [4+2]-cycloaddition reactions with olefins catalyzed by PtCl4 and AuCl3 under mild conditions have been developed. Good to excellent yields (up to 99%) and diastereoselectivity (up to >99:1) of the chromans were obtained. PtCl4 was found to be effective and compatible with various functional groups present in the substrates. A mechanism accounting for its catalytic cycle is proposed and discussed.

Generation of ortho-quinone methides by p-TsOH on silica and their hetero-Diels-Alder reactions with styrenes

(Chemical Equation Presented) 2-Arylchromans were readily prepared from the hetero-Diels-Alder reactions of styrenes with the ortho-quinone methides (o-QMs) which, in turn, were generated by treating the MOM-protected benzylacetate derivatives with p-TsOH immobilized on silica (PTS-Si) in toluene under mild conditions (0°C to rt). The corresponding chromans were obtained in moderate to excellent yields (42-97%) and in moderate to excellent diastereoselectivity (up to >99:1).

Synthesis of a new series of chiral tri- and tetradentate ligands and their application in titanium-catalyzed pinacol coupling reaction

A variety of chiral tridentate and tetradentate ligands, related to each other through stereoelectronic relationship have been synthesized. Homochiral diols and amino alcohols have been used for this purpose. Titanium complexes of these ligands have been prepared and examined for enantioselective pinacol coupling reaction.

Highly enantioselective aza-Morita-Baylis-Hillman reaction with a bisphenol-based bifunctional organocatalyst

Newly developed phosphino-bisphenol 1c was found to be an efficient organocatalyst for the aza-Morita-Baylis-Hillman reaction. High enantioselectivity up to 96% ee was obtained with catalyst loading of 1 mol %.

Bicyclic aromatic compounds and pharmaceutical/cosmetic compositions comprised thereof

Novel pharmaceutically/cosmetically-active bicyclic aromatic compounds have the structural formula (I): in which Ar1 is a radical having one of the structural formulae (a)-(c): Ar2 is a radical having one of the following formulae (d)-(h): and X is a radical having one of the following formulae (i)-(l): and are useful for the treatment of a wide variety of disease states, whether human or veterinary, for example dermatological, rheumatic, respiratory, cardiovascular and ophthalmological disorders, as well as for the treatment of mammalian skin and hair conditions/disorders.

Radicicol derivatives

Radicicol derivatives represented by the following formula (I) having tyrosine kinase inhibition activity or pharmacologically acceptable salts thereof: wherein R1and R2are the same or different, and each represents hydrogen, alkanoy