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Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)-, also known as 2'-chloro-N-(2-aminophenyl)acetophenone, is a chemical compound with the molecular formula C16H14ClNO. It is a ketone derivative that features an amino group attached to a phenyl ring and a chlorine-substituted phenyl ring. This unique structure endows it with potential applications in various fields, particularly in pharmaceutical and organic chemistry, due to its versatile chemical properties.

141034-45-9

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141034-45-9 Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence of both an amino group and a chlorine-substituted phenyl ring allows for the development of new drugs with specific therapeutic properties. Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)can be utilized in the creation of novel molecules with potential applications in treating various diseases and medical conditions.
Used in Organic Chemistry Research:
In the field of organic chemistry, Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)serves as a valuable research tool. Its unique structure allows chemists to explore new synthetic pathways and reactions, leading to the discovery of novel compounds with potential applications in various industries. Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)can be used to study the reactivity of functional groups and to develop new synthetic methodologies.
Used in Chemical Synthesis:
Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)is used as a building block in the synthesis of complex organic molecules. Its versatile structure allows for the formation of various functional groups and the creation of new chemical entities. Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)can be employed in the development of new materials, dyes, and other specialty chemicals.
Used in Analytical Chemistry:
Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)can be utilized as a reference compound in analytical chemistry. Its unique structure and properties make it suitable for the development of new analytical methods and techniques, such as chromatography, spectroscopy, and mass spectrometry. Ethanone, 1-(2-aminophenyl)-2-(2-chlorophenyl)can be used to calibrate instruments and to validate analytical procedures.

Check Digit Verification of cas no

The CAS Registry Mumber 141034-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,3 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141034-45:
(8*1)+(7*4)+(6*1)+(5*0)+(4*3)+(3*4)+(2*4)+(1*5)=79
79 % 10 = 9
So 141034-45-9 is a valid CAS Registry Number.

141034-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-aminophenyl)-2-(2-chlorophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(2-Aminophenyl)-2-(2-chlorophenyl)ethan-1-one

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:141034-45-9 SDS

141034-45-9Relevant academic research and scientific papers

Cyclic Amidines Part 27. An Unambiguous Synthesis of 5,10,14c-Triazabenzo naphthanthracene by a Palladium Catalysed Cyclodehalogenation

Upton, Christopher

, p. 951 - 965 (2007/10/02)

An unambiguous route to the title triazabenzonaphthanthracene (5) is reported via a palladium-catalyzed cyclodehalogenation of the 6-chloro-7-(2-chlorobenzylidene)-benzanthracene (10) avoiding high temperature reactions and the possibility of skeletal rea

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