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18859-48-8

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18859-48-8 Usage

Type of compound

Ketone derivative A class of organic compounds that have a carbonyl functional group (C=O) bonded to two carbon-containing groups.

Structural components

Phenyl group and chlorophenoxy group The compound has a phenyl group (a ring of six carbon atoms with a hydrogen atom attached to each) and a chlorophenoxy group (a phenyl ring with an ether and chlorine atom attached) attached to the carbon chain.

Usage

Intermediate in synthesis of pharmaceuticals and agrochemicals It is commonly used as a starting material or building block in the production of various pharmaceutical and agrochemical compounds.

Versatile reactivity

Organic synthesis and research The compound is widely used in organic synthesis and research due to its ability to react with a variety of other compounds and its potential to modify their properties.

Potential applications

Pharmaceutical or agrochemical ingredient 2-(4-chlorophenoxy)-1-phenylethanone may have possible uses as an ingredient in pharmaceutical or agrochemical products, but further research is needed to determine its specific applications and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 18859-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,5 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18859-48:
(7*1)+(6*8)+(5*8)+(4*5)+(3*9)+(2*4)+(1*8)=158
158 % 10 = 8
So 18859-48-8 is a valid CAS Registry Number.

18859-48-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenoxy)-1-phenylethanone

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18859-48-8 SDS

18859-48-8Relevant articles and documents

Synthesis, X-ray crystal structure and theoretical calculations of antileishmanial neolignan analogues

Do Nascimento, Josenaide P.,Santos, Lourivaldo S.,Santos, Regina Helena A.,Tozzo, E?rica,Ferreira, Janaina G.,Do Carmo, Maria Carolina L.,Brasil, Davi S. B.,Alves, Cla?udio N.

, p. 1825 - 1837 (2010)

The synthesis and X-ray crystal diffraction structure of two analogues of neolignans, 2-(4-chlorophenyl)-1-phenylethanone (20) and 2-[(4-chlorophenyl) thio]-1-(3,4-dimethoxyphenyl)propan-1-one (12) is described. The compound 12 presents activity against i

Palladium-catalyzed α-arylation of aryloxyketones for the synthesis of 2,3-Disubstituted benzofurans

Lee, Jin Ho,Kim, Myungock,Kim, Ikyon

, p. 6153 - 6163 (2014/07/21)

A highly efficient palladium-catalyzed α-arylation of aryloxyketones has been developed, allowing for facile installation of various (hetero)aryl groups at C2 position in good to excellent yields. Subsequent cyclodehydration of the resulting α-arylated ar

ALLOSTERIC PROTEIN KINASE MODULATORS

-

Page/Page column 143, (2010/04/30)

The invention provides specific small molecule compounds that allosterically regulate the activity or modulate protein-protein interactions of AGC protein kinases and the Aurora family of protein kinases, methods for their production, pharmaceutical compositions comprising same, and their use for preparing medicaments for the treatment and prevention of diseases related to abnormal activities of AGC protein kinases or of protein kinases of the Aurora family.

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