67031-41-8

Usage

Uses

Used in Fragrance Industry:
1-(3,4-Dimethoxyphenyl)-2-methyl-1-propanol is used as a fragrance ingredient for its floral and woody aroma, making it a popular choice in the creation of perfumes and personal care products. Its unique scent profile contributes to the overall appeal and character of these products, enhancing the sensory experience for consumers.
Used in Cosmetic Industry:
In the cosmetic industry, 1-(3,4-Dimethoxyphenyl)-2-methyl-1-propanol is utilized as an ingredient for its pleasant scent and ability to blend well with other components in cosmetic formulations. Its inclusion in these products helps to create a more enjoyable and luxurious experience for users.
Used in Organic Synthesis:
Due to its unique chemical structure and reactivity, 1-(3,4-Dimethoxyphenyl)-2-methyl-1-propanol may also be employed in the synthesis of other organic compounds. Its versatility in chemical reactions allows it to serve as a valuable building block or intermediate in the development of various chemical products.

InChI:InChI=1/C12H18O3/c1-8(2)12(13)9-5-6-10(14-3)11(7-9)15-4/h5-8,12-13H,1-4H3

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 75-26-3 isopropyl bromide 
• 920-39-8 isopropylmagnesium bromide 
• 1068-55-9 isopropylmagnesium chloride 

Downstream Products

• 14046-55-0 isobutyryl-3,4-dimethoxybenzene 
• 20850-49-1 2-(3,4-dimethoxyphenyl)-3-methylbutyronitrile 
• 349078-67-7 3-(3,4-dimethoxyphenyl)-3-hydroxy-4-methylpentanenitrile 
• 89950-18-5 1-(2,4-dimethoxyphenyl)-1-(3,4-dimethoxyphenyl)-2,2-dimethylethane 

Relevant academic research and scientific papers

Copper-catalyzed iminohalogenation of γ, δ-unsaturated oxime esters with halide salts: Synthesis of 2-halomethyl pyrrolines

A copper-catalyzed iminohalogenation of unactivated alkenes of γ, δ-unsaturated oxime esters is achieved by using readily available halide salts. Utilizing this protocol, a sequence of structurally diversiform 2-halomethyl pyrrolines are efficiently synthesized and a mechanism involving iminyl radical intermediates, which were initiated by Cu(I) species, was proposed.

Silver-promoted cascade radical cyclization of γ,δ-unsaturated oxime esters with P(O)H compounds: synthesis of phosphorylated pyrrolines

A cascade radical cyclization was realized for the first silver-promoted imino-phosphorylation of γ,δ-unsaturated oxime esters, which provided a step-economical and redox-neutral route to access a variety of phosphorylated pyrrolines in good to excellent yields. Moreover, a new bulky trivalent phosphine ligand with a pyrroline motif was obtained through a deoxidation process.

FUNGICIDAL COMPOSITION CONTAINING ACID AMIDE DERIVATIVE

Conventional many fungicidal compositions have had practical problems such that either a preventive effect or a curing effect is inadequate, the residual effect tends to be inadequate, or the controlling effect against plant diseases tends to be inadequat

Method for preparing a benzylic-type ether

The invention concerns a method for preparing a benzylic-type ether from an aromatic compound. The inventive method for preparing a benzylic-type ether from an aromatic compound is characterised in that it consists in: in a first step, acylating an aromatic compound by reacting said aromatic compound with an acylating agent, in the presence of an efficient amount of zeolite or a Friedel-Crafts catalyst leading to a ketonic compound; in a second step, reducing the carbonyl group into carbinol leading to a benzylic alcohol; in a third step, etherifying the hydroxyl group, by reacting the benzylic alcohol with another alcohol, in the presence of an efficient amount of zeolite.

Enzyme-mediated synthesis of (S)- And (R)-verapamil

A lipase-mediated synthesis of (S)- And (R)-verapamil is described. The key steps of the synthetic sequence are the enantioselective acetylation, mediated by Lipase PS, of allylic alcohol (Z)-(±)-2, affording the acetate derivative (Z,R)-(-)-3 (ee 92%) and the Ireland-Claisen rearrangement of this latter and of its enantiomer (Z,S)-(+)-3 (ee 92%) to afford acid derivatives (E,R)-(-)-4 (ee 94%) and (E,S)-(+)-4 (ee 93%), precursors of (S)- and (R)-verapamil, respectively.

In vitro evaluation of antifungal properties of phenylpropanoids and related compounds acting against dermatophytes

Thirty-four arylpropanoids and related compounds were evaluated in vitro for antifungal properties. Among them, 22 phenyl-, 4 naphthyl-, and 4 phenanthrylpropanoids; naphthalene; phenanthrene; and 2-chloro-1-hexyl-1- propanone were tested against dermatop