82935-36-2

Usage

Uses

Used in Pharmaceutical Industry:
2,6-Diethoxybenzoic acid 97 is used as an intermediate in the synthesis of various pharmaceuticals for its unique properties and reactivity.
Used in Dye Industry:
This chemical compound is used in the production of dyes, contributing to the coloration of various products.
Used in Fragrance Industry:
2,6-Diethoxybenzoic acid 97 is used as a fragrance ingredient in personal care products and cosmetics due to its mild and pleasing odor.
Used in Organic Compounds Synthesis:
It serves as an intermediate in the synthesis of other organic compounds, expanding its application potential across different industries.

InChI:InChI=1/C11H14O4/c1-3-14-8-6-5-7-9(15-4-2)10(8)11(12)13/h5-7H,3-4H2,1-2H3,(H,12,13)

Upstream product

• 303-07-1 2,6-Dihydroxybenzoic acid 

Downstream Products

• 82935-45-3 2,6-Diethoxy-N-(1-ethyl-pyrrolidin-2-ylmethyl)-benzamide 
• 82935-48-6 3-Chloro-2,6-diethoxy-N-(1-ethyl-pyrrolidin-2-ylmethyl)-benzamide 
• 82935-46-4 2-<(3-bromo-2,6-diethoxybenzamido)methyl>-1-ethylpyrrolidine 
• 82935-47-5 (S)-(-)-3-bromo-N-<(1-ethyl-2-pyrrolidynyl)methyl>-2,6-diethoxybenzamide 
• 2049-73-2 2,4-diethoxybenzene 
• 17715-68-3 2-chloro-1,3-diethoxybenzene 
• 1435943-57-9 2-bromo-1,3-diethoxybenzene 

Relevant academic research and scientific papers

Method for producing o-alkoxybenzoic acid

o-Methoxy benzoic acid is produced by reacting chlorobenzoic acids having at least one chlorine atom at least at the ortho position with lower alcohol in the presence of a copper salt and a lower alkyl as a catalyst under moderate reaction conditions. o-Methoxy benzoic acid is useful as an intermediate for pharmaceutical, agricultural chemicals, and the like.

Potential Neuroleptic Agents. 2,6-Dialkoxybenzamide Derivatives with Potent Dopamine Receptor Blocking Activities

A series of some novel N-(1-ethyl-2-pyrrolidinylmethyl)benzamides was synthesized and tested for dopamine receptor blockade in vivo by the ability to block the apomorphine syndrome in the rat.Several compounds were considerably more potent than sulpiride as dopamine receptor blockers and displayed low liability to induce extrapyramidal side effects (catalepsy) in the rat.The blockade of dopamine receptor activity in vivo was mainly confined to the levorotatory isomers having the S absolute configuration.The structure-activity relationships are discussed.