22072-50-0

Usage

Chemical Structure

C10H12O2

Type of Compound

Organic compound

Functional Group

Ketone

Structure

Benzene ring present
Methoxy group attached to the fourth carbon of the benzene ring
Methyl group attached to the first carbon of the ethanone chain

Usage

Fragrance ingredient
Used in manufacturing perfumes, soaps, and other scented products

Scent

Sweet, floral, and woody

Physical State

Clear, colorless liquid at room temperature

Solubility

Insoluble in water
Soluble in organic solvents such as ethanol and acetone

Safety Precautions

May cause irritation to skin, eyes, and respiratory system if exposed in high concentrations
Handle with caution

InChI:InChI=1/C10H12O2/c1-8(11)10-5-3-9(4-6-10)7-12-2/h3-6H,7H2,1-2H3

Upstream product

• 917-64-6 methyl magnesium iodide 
• 1515-85-1 4-(methoxymethyl)benzonitrile 
• 27490-32-0 tributyl(methoxymethyl)stannane 
• 99-90-1 para-bromoacetophenone 
• 14490-45-0 4-(2-methyl-1,3-dioxolan-2-yl)benzaldehyde 
• 78906-12-4 2-methyl-2-(4-hydoxymethylphenyl)-1,3-dioxolyn 
• 874-89-5 4-Cyanobenzyl alcohol 
• 1515-88-4 1-bromo-4-methoxymethylbenzene 
• 910251-11-5 potassium trifluoro(methoxymethyl)boranuide 

Downstream Products

• 66190-31-6 (+)-1-(4-methoxymethylphenyl)ethanol 
• 66190-31-6 (-)-1-(4-methoxymethylphenyl)ethanol 
• 137684-23-2 4-(methoxymethyl)phenylglyoxal 
• 1610345-76-0 N-(2,2-dimethoxyethyl)-2,2,2-trifluoro-N-(1-(4-(methoxymethyl)phenyl)ethyl)ethanamine 
• 1610345-74-8 2,2-dimethoxy-N-(1-(4-(methoxymethyl)phenyl)ethyl)ethanamine 

Relevant academic research and scientific papers

1,2,4-TRIAZINE-4-AMINE DERIVATIVES

According to the invention there is provided a compound of formula A1 which may be useful in the treatment of a condition or disorder ameliorated by the inhibition of the A1- A2b or, particularly, the A2a receptor wherein the compound of formula A1 has the structure, wherein, A represents Cy1 or HetA; Cy1 represents a 5- to 14-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one, two or three rings, which Cy1 group is optionally substituted by one or more R4a substituents; HetA represents a 5- to 14-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one, two or three rings and which HetA group is optionally substituted by one or more R4b substituents; B represents a Cy2 or HetB; Cy2 represents a 3- to 10-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one or two rings, which Cy2 group is optionally substituted by one or more R4c substituents; HetB represents a 3- to 10-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one or two rings and which HetB group is optionally substituted by one or more R4d substituents.

Experimental investigations of a partial Ru-O bond during the metal-ligand bifunctional addition in noyori-type enantioselective ketone hydrogenation

The transition state for the metal-ligand bifunctional addition step in Noyori's enantioselective ketone hydrogenation was investigated using intramolecular trapping experiments. The bifunctional addition between the Ru dihydride trans-[Ru((R)-BINAP)(H)2((R,R)-dpen)] and the hydroxy ketone 4-HOCH2C6H4(CO)CH3 at -80 °C exclusively formed the corresponding secondary ruthenium alkoxide trans-[Ru((R)-BINAP)(H)(4-HOCH2C6H4CH(CH 3)O)((R,R)-dpen)]. Combined with the results of control experiments, this observation provides strong evidence for the formation of a partial Ru-O bond in the transition state.

HYDROXYMETHYLBORON COMPOUNDS

The present invention provides compounds which are useful as safe substitutes for the organotin reagent used in coupling reaction for the oxymethylation of aromatic rings, such as alkoxymethylation or hydroxymethylation, with a palladium catalyst and which can dispense with chromatographic purification with silica gel in the production and are suitable for mass production; and compounds applicable even to the oxymethylation of aromatic ring substrates which do not permit coupling reaction by conventional technique or have low reactivity.

A NOVEL METHOXYMETHYLATION OF ARYL BROMIDE BY METHOXYMETHYLTRIBUTYLTIN IN THE PRESENCE OF PALLADIUM COMPLEX

The reaction of aryl bromides with methoxymethyltributyltin in the presence of a catalytic amount of dichlorobis(triphenylphosphine)palladium was found to give arylmethyl methyl ether.The reaction is a novel aromatic methoxymethylation.