15422-18-1

Basic information

• Product Name: 1-(3-CHLOROPHENOXY)-2-PROPANONE
• Synonyms: 1-(3-CHLOROPHENOXY)-2-PROPANONE
• CAS NO: 15422-18-1
• Molecular Formula: C₉H₉ClO₂
• Molecular Weight: 184.62
• Mol File: 15422-18-1.mol

Chemical Properties

• Boiling Point: 268.2°C at 760 mmHg
• Flash Point: 114.2°C
• Appearance: /
• Density: 1.187g/cm³
• Vapor Pressure: 0.00781mmHg at 25°C
• Refractive Index: 1.517
• CAS DataBase Reference: 1-(3-CHLOROPHENOXY)-2-PROPANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-CHLOROPHENOXY)-2-PROPANONE(15422-18-1)
• EPA Substance Registry System: 1-(3-CHLOROPHENOXY)-2-PROPANONE(15422-18-1)

Safety Data

• Hazardous Substances Data: 15422-18-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-(3-CHLOROPHENOXY)-2-PROPANONE is used as an intermediate for the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(3-CHLOROPHENOXY)-2-PROPANONE serves as an intermediate in the production of agrochemicals, which are essential for enhancing crop protection and agricultural productivity.
Used in Organic Synthesis:
1-(3-CHLOROPHENOXY)-2-PROPANONE is utilized as a chemical building block in organic synthesis, playing a vital role in the creation of diverse organic compounds.
Used in Perfume and Flavoring Industry:
1-(3-CHLOROPHENOXY)-2-PROPANONE is also employed in the production of perfumes and flavorings, where its unique properties contribute to the development of distinct scents and tastes.

InChI:InChI=1/C9H9ClO2/c1-7(11)6-12-9-4-2-3-8(10)5-9/h2-5H,6H2,1H3

Upstream product

• 108-43-0 3-monochlorophenol 
• 78-95-5 chloroacetone 
• 67-64-1 acetone 
• 75-56-9 methyloxirane 

Downstream Products

• 18621-36-8 (3-Chlor-phenoxy)-aceton-dimethyl-ketal 

Relevant articles and documents

Selective Cross-Dehydrogenative C(sp3)-H Arylation with Arenes

Selective C(sp3)-C(sp2) bond construction is of central interest in chemical synthesis. Despite the success of classic cross-coupling reactions, the cross-dehydrogenative coupling between inert C(sp3)-H and C(sp2)-H bonds represents an attractive alternative toward new C(sp3)-C(sp2) bonds. Herein, we establish a selective inter-and intramolecular C(sp3)-H arylation of alcohols with nondirected arenes that thereby provides a general pathway to access a wide range of β-arylated alcohols, including tetrahydronaphthalen-2-ols and benzopyran-3-ols, with high to excellent chemo-and regioselectivity.

TBAI/TBHP mediated oxidative cross coupling of ketones with phenols and carboxylic acids: Direct access to benzofurans

TBAI/TBHP mediated oxidative cross coupling of phenols and carboxylic acids with ketones has been reported under metal-free, base free, solvent free conditions enabling environmentally benign synthesis of aryloxyketones, acyloxy ketones and benzofurans. Phenoxyketones and acyloxylcarbonyl compounds were synthesized in good to high yields, where as benzofurans were synthesized in moderate yields. This method is operationally simple, works under mild conditions, using commercially available as well as inexpensive TBAI and an oxidant TBHP.

A (different) bright ammonia amide carbamate derivative and application thereof (by machine translation)

The invention belongs to the field of plant, relates to a general formula (I) is shown in a (different) bright ammonia amide carbamate derivatives and their pharmaceutically acceptable salt, wherein substituent R has the definition given in the specification, the invention also relates to the general formula (I) preparation of compounds of the, specifically for the preparation of the intermediate of its development and application of plant disease control. (by machine translation)