6642-39-3

Usage

Physical state

Colorless to pale yellow liquid

Odor

Strong, sweet, and spicy

Natural occurrence

Found in essential oils such as clove oil, nutmeg, and cinnamon

Uses in the food and beverage industry

Flavoring agent

Uses in perfumes and cosmetics

Fragrance

Traditional medicinal uses

Analgesic, antiseptic, and anti-inflammatory properties

Application in dentistry

Numbing effect in dental procedures

Pharmacological properties

Potential applications in the pharmaceutical industry

InChI:InChI=1/C11H16O2/c1-8(2)11(12)9-6-4-5-7-10(9)13-3/h4-8,11-12H,1-3H3

Upstream product

• 920-39-8 isopropylmagnesium bromide 
• 111289-42-0 bis(2-methoxybenzoyl) telluride 
• 74786-53-1 1-(2-methoxyphenyl)-2-methylpropan-1-one 
• 75-30-9 2-iodo-propane 
• 135-02-4 ortho-anisaldehyde 
• 2040-20-2 4-methoxyisobutyrophenone 
• 16750-63-3 2-methoxyphenylmagnesium bromide 
• 78-84-2 isobutyraldehyde 

Downstream Products

• 499236-03-2 1-(1-Chloro-2-methylpropyl)-2-methoxybenzene 
• 91967-51-0 1-isobutyl-2-methoxybenzene 
• 4167-75-3 2-isobutylphenol 
• 6026-72-8 1-(2-methoxyphenyl)-2-methylprop-1-ene 

Relevant academic research and scientific papers

Bimetallic Catalysis: Asymmetric Transfer Hydrogenation of Sterically Hindered Ketones Catalyzed by Ruthenium and Potassium

An efficient protocol for the asymmetric reduction of sterically hindered ketones under transfer-hydrogenation conditions was developed. The corresponding chiral alcohols were obtained in good to excellent yields with enantiomeric excess values up to 99 %. The role of the cation associated with the base present in the reduction reaction was investigated. In contrast to previous studies on this catalyst system, potassium ions rather than lithium ions significantly enhanced the reaction outcome.

Diaroyl tellurides: Synthesis, structure and NBO analysis of (2-MeOC 6H4CO)2Te - comparison with its sulfur and selenium isologues. The first observation of [MgBr][R(C=Te)O] salts

A series of aromatic diacyl tellurides were prepared in moderate to good yields by the reactions of sodium or potassium arenecarbotelluroates with acyl chlorides in acetonitrile. X-ray structure analyses and theoretical calculations of 2-methoxybenzoic an

Reaction of secondary and tertiary aliphatic halides with aromatic aldehydes mediated by chromium(II): a selective cross-coupling of alkyl and ketyl radicals

Takai-Utimoto reactions with secondary and tertiary aliphatic halides usually failed according to previous reports. Now, significant improvements could be achieved, and especially secondary aliphatic halides can be coupled to aromatic aldehydes in yields of up to >95%. A variety of processes are competing with the desired one, and thus conditions must be adapted to the nature of the aldehyde as well as the aliphatic halide used, as the outcome of these reactions is strongly affected by the putative radical intermediates.

3-PHENOXY-4-PYRIDAZINOL DERIVATIVE AND HERBICIDE COMPOSITION CONTAINING THE SAME

A compound represented by the formula: wherein R1 represents a hydrogen atom, a halogen atom, alkyl group, etc., ???R2 represents a hydrogen atom, a halogen atom, alkyl group, etc., ???R3, R4, R5, R6 and R7 each independently represent a hydrogen atom, a halogen atom, a substitutable alkyl group, a substitutable alkenyl group, alkynyl group, a substitute-able cycloalkyl group, etc., or adjacent two of R3, R4, R5, R6 and R7 may together with the carbon atoms to which the respective substituents are bonded form a ring which may be substituted, ???m and n each independently represent 0 or 1, a salt thereof or an ester derivative thereof; an agricultural chemical containing the same as an active ingredient; and a herbicidal composition containing the compound and a second herbicidally active compound as active ingredients.