480439-42-7

Basic information

• Product Name: 2,6-DIETHOXYBENZOYL CHLORIDE
• Synonyms: 2,6-DIETHOXYBENZOYL CHLORIDE
• CAS NO: 480439-42-7
• Molecular Formula: C₁₁H₁₃ClO₃
• Molecular Weight: 228.67212
• Mol File: 480439-42-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-DIETHOXYBENZOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIETHOXYBENZOYL CHLORIDE(480439-42-7)
• EPA Substance Registry System: 2,6-DIETHOXYBENZOYL CHLORIDE(480439-42-7)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• Hazardous Substances Data: 480439-42-7(Hazardous Substances Data)

Usage

General Description

2,6-Diethoxybenzoyl chloride is a chemical compound with the formula C11H13ClO3. It is a benzoyl chloride derivative that is commonly used as an intermediate in the production of pharmaceuticals and agrochemicals. 2,6-DIETHOXYBENZOYL CHLORIDE is a clear, colorless liquid with a strong, pungent odor. It is highly reactive and is commonly used as a reagent in organic chemistry reactions, such as in the synthesis of esters and amides. It should be handled with care and kept away from moisture and sources of ignition due to its flammable and corrosive properties.

Upstream product

• 82935-36-2 2,6-diethoxybenzoic acid 
• 303-07-1 2,6-Dihydroxybenzoic acid 
• 92157-15-8 2,6-Diaethoxy-benzoesaeure-aethylester 

Relevant articles and documents

CYCLOPENTYLBENZAMIDE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF PSYCHOTIC AND COGNITIVE DISORDERS

The present invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein n, L, X, Ra, Rb, R1, R2 and R3 their preparation, pharmaceutical compositions containing them and their use in therapy.

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.