1137-71-9

Usage

Uses

Used in Flavor and Fragrance Industry:
1-(3,4-DIETHOXYPHENYL)ETHANONE is used as a flavoring agent and fragrance for its sweet, floral scent, enhancing the sensory experience of various consumer products.
Used in Organic Synthesis:
1-(3,4-DIETHOXYPHENYL)ETHANONE is used as a versatile building block in organic chemistry for the synthesis of pharmaceuticals and other organic compounds, contributing to the development of new chemical entities.
Used in Pharmaceutical Industry:
1-(3,4-DIETHOXYPHENYL)ETHANONE is used in the synthesis of pharmaceuticals due to its potential as a precursor for the development of new drugs.
Used in Medical Research:
1-(3,4-DIETHOXYPHENYL)ETHANONE is studied for its potential anti-inflammatory and antimicrobial properties, indicating its use in medical research for the development of new treatments and therapies.

InChI:InChI=1/C12H16O3/c1-4-14-11-7-6-10(9(3)13)8-12(11)15-5-2/h6-8H,4-5H2,1-3H3

Upstream product

• 64-67-5 diethyl sulfate 
• 1197-09-7 1-(3,4-dihydroxyphenyl)ethan-1-one 
• 2050-46-6 1,2-diethoxybenzene 
• 64-19-7 acetic acid 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Downstream Products

• 38464-04-9 3,4-diethoxy-phenyl-acetic acid 
• 985-12-6 1-(3,4-diethoxybenzylidene)-6,7-diethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 6298-46-0 N-(3,4-diethoxyphenylacetyl)-β-(3,4-diethoxyphenyl)ethylamine 
• 61381-04-2 2-(3,4-diethoxyphenyl)ethylamine 
• 54088-62-9 (6,7-diethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)(3,4-diethoxyphenyl)methanone 
• 117379-78-9 (E)-4-(3,4-Diethoxy-phenyl)-4-oxo-but-2-enoic acid 

Relevant academic research and scientific papers

Novel method for preparing drotaverine hydrochloride intermediate

The invention discloses a novel method for preparing a drotaverine hydrochloride intermediate, belonging to the technical field of medicine synthesis. The preparation method comprises the following steps: preparing an intermediate 3,4-diethoxyphenylacetic acid with 1,2-diethoxybenzene as a raw material, and preparing the intermediate 3,4-diethoxyphenylacetamide with 3,4-diethoxyphenylacetic acid as a raw material. According to the novel process for preparing the drotaverine hydrochloride intermediate, a method for directly preparing 3,4-diethoxyphenylacetic acid and 3,4-diethoxyphenylethylamine is adopted, and a process for preparing 3,4-diethoxyphenylacetonitrile is avoided, so a reaction step of using sodium cyanide is avoided.

Aluminum dodecatungstophosphate (AlPW12O40) as a non-hygroscopic Lewis acid catalyst for the efficient Friedel-Crafts acylation of aromatic compounds under solvent-less conditions

Stable and non-hygroscopic aluminum dodecatungstophosphate (AlPW 12O40), which is prepared easily from cheap and commercially available compounds was found to be an effective catalyst for Friedel-Crafts acylation reactions using carboxylic acids, acetic anhydride and benzoyl chloride in the absence of solvent under mild reaction conditions.

Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers

The acetylation of aryl ethers using acetic anhydride in the presence of zeolites under modest conditions in a solvent-free system gave the corresponding para-acetylated products in high yields. The zeolite can be recovered, regenerated and reused to give almost the same yields as that given when fresh zeolite is used.

Solvent-free Friedel-Crafts acylation of aromatic compounds with carboxylic acids in the presence of trifluoroacetic anhydride and aluminum dodecatungstophosphate

The stable and non-hygroscopic aluminum dodecatungstophosphate (AlPW12O40), was found to be an effective catalyst (3 mol%) for the solvent-free Friedel-Crafts acylation of aromatic compounds with carboxylic acids in the presence of trifluoroacetic anhydride under mild reaction conditions.

Triazine derivatives, a process for preparing the derivatives, and herbicides containing the derivatives as the effective component

A triazine derivative represented by the general formula: STR1 wherein R1 and R2 are each an alkyl group having 1 to 4 carbon atoms, and X1 and X2 are each a halogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, or an alkylthio group having 1 to 4 carbon atoms. This invention also provides a process for efficiently preparing said triazine derivative and a herbicide containing said triazine derivative as effective component.