34577-33-8

Usage

Appearance

Colorless liquid

Odor

Minty, pine-like

Industry use

Flavor and fragrance industry

Found in

Essential oils (e.g., spearmint and caraway)

Application

Flavoring agent in food and beverages

Potential pharmaceutical applications

Anti-inflammatory and antimicrobial properties

Upstream product

• 111823-36-0 [(3,5-dimethylphenyl)methyl]magnesium bromide 
• 67-64-1 acetone 
• 105337-18-6 ethyl 2-(3,5-dimethylphenyl)acetate 
• 75-16-1 methylmagnesium bromide 
• 108-67-8 1,3,5-trimethyl-benzene 

Downstream Products

• 34586-21-5 4-Nitro-benzenecarboperoxoic acid 2-(3,5-dimethyl-phenyl)-1,1-dimethyl-ethyl ester 
• 34586-06-6 1-(3,5-Dimethyl-phenyl)-2-methyl-prop-2-yl-hydroperoxide 
• 868049-83-6 N-[2-(3,5-dimethylphenyl)-1,1-dimethyl-ethyl]formamide 

Relevant academic research and scientific papers

Pd(II)-catalyzed hydroxyl-directed C-H olefination enabled by monoprotected amino acid ligands

A novel Pd(II)-catalyzed ortho-C-H olefination protocol has been developed using spatially remote, unprotected tertiary, secondary, and primary alcohols as the directing groups. Mono-N-protected amino acid ligands were found to promote the reaction, and an array of olefin coupling partners could be used. When electron-deficient alkenes were used, the resulting olefinated intermediates underwent subsequent Pd(II)-catalyzed oxidative intramolecular cyclization to give the corresponding pyran products, which could be converted into ortho-alkylated alcohols under hydrogenolysis conditions. The mechanistic details of the oxidative cyclization step are discussed and situated in the context of the overall catalytic cycle.

Novel medicaments for the treatment of respiratory diseases

The present invention relates to the use of the compounds of general formula 1 wherein the groups R1, R2 and R3 may have the meanings given in the claims and in the specification, for preparing a pharmaceutical composition

Aerosol formulation for the inhalation of beta-agonists

The present invention relates to a propellant-free aerosol formulation which [contains] one or more compounds of general formula 1 wherein the groups R1, R2, R3 and X? may have the meanings given in the claims a

PHOTOCHEMICAL OXIDATION AND DIMERIZATION OF ALKYLBENZENES. SELECTIVE REACTIONS OF THE ALKYL SIDE GROUPS

Irradiations of alkylbenzene compounds in an oxygen atmosphere result exclusively in oxidation reactions, while in a less oxidative environment dimerization processes predominate.Under all conditions studied, the reactions took place only at one benzyl position.