181297-72-3

Usage

General Description

2-(3-chlorophenoxy)benzenecarbaldehyde is a chemical compound with the molecular formula C13H9ClO2. It is a white to light yellow crystalline powder that is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of dyes and other organic compounds. This chemical is a benzaldehyde derivative, and it possesses a chlorophenoxy group that enhances its reactivity and selectivity in various chemical reactions. It is important to handle 2-(3-CHLOROPHENOXY)BENZENECARBALDEHYDE with caution as it may cause irritation to the skin, eyes, and respiratory system if not properly handled.

Upstream product

• 126644-71-1 1-<(tert-butyldimethylsilyl)oxy>-3-chlorobenzene 
• 446-52-6 2-Fluorobenzaldehyde 
• 108-43-0 3-monochlorophenol 

Downstream Products

• 1005763-17-6 1-(2-(3-chlorophenoxy)phenyl)-N,N-dimethylmethanamine 
• 126165-45-5 3-chlorophenyl 2-hydroxybenzoate 

Relevant academic research and scientific papers

Pyrimidine onium compound and application thereof

The invention relates to a pyrimidine onium compound, nitride oxides, salt of the nitride oxides and a composition comprising the compound. The invention further relates to an application of the compound to plant pest control.

HETEROARYL RHEB INHIBITORS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same. Compositions comprising a compound of this invention or a pharmaceutically acceptable derivative thereof and a pharmaceutically acceptable carrier, adjuvant, or vehicle. The amount of the compound in compositions of this invention is such that it is effective to measurably inhibit Rheb, in a biological sample or in a patient.

1-(2-Phenoxyphenyl)methanamines: SAR for dual serotonin/noradrenaline reuptake inhibition, metabolic stability and hERG affinity

A novel series of 1-(2-phenoxyphenyl)methanamines is disclosed, which possess selective dual 5-HT and NA reuptake pharmacology. Analogues with good human in vitro metabolic stability, hERG selectivity and passive membrane permeability were identified.

P(i-BuNCH2CH2)3N: An efficient promoter for the nucleophilic aromatic substitution reaction of aryl fluorides with aryl TBDMS (or TMS) ethers

(Chemical Equation Presented) The nucleophilic aromatic substitution reaction between electron-deficient aryl fluorides and aryl TBDMS (or TMS) ethers has been shown to be efficiently promoted by proazaphosphatranes such as P(i-BuNCH2CH2)3N (3). Excellent yields of diaryl ether products were obtained under unusually mild conditions.

Anti-neurodegeneratively active 10-aminoaliphatyl-dibenzi ?b,f! oxepines

Base-substituted debenz?b,f!oxepines of formula I STR1 wherein alk is a divalent aliphatic radical, R is an amino group that is unsubstituted or mono- or di-substituted by monovalent aliphatic and/or araliphatic radicals or disubstituted by divalent aliph