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
• Article Data: 3

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

General Description

1-(3-CHLOROPHENOXY)-2-PROPANONE is a chemical compound with the molecular formula C9H9ClO2. It is a pale yellow liquid with a molecular weight of 184.62 g/mol. 1-(3-CHLOROPHENOXY)-2-PROPANONE is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a chemical building block in organic synthesis and in the production of perfumes and flavorings. The presence of the chlorophenyl group in this compound makes it useful in the development of various organic compounds. However, it is important to handle this chemical with proper safety precautions, as it can be hazardous if not handled and used appropriately.

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 
• 75-56-9 methyloxirane 
• 67-64-1 acetone 
• 78-95-5 chloroacetone 

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.

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)