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[2-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate is a chemical compound with the molecular formula C16H13ClO3. It is an ester derived from chloroacetic acid and an α-oxo ketone, known for its use in organic synthesis as a reagent for various reactions, including carboxylation and esterification. [2-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate also holds potential in the pharmaceutical industry as a building block for the synthesis of biologically active compounds. However, it is crucial to handle [2-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate with care due to its nature as a chloroacetic acid ester, which may pose health hazards if not properly managed.

4376-28-7

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4376-28-7 Usage

Uses

Used in Organic Synthesis:
[2-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate is used as a reagent in organic synthesis for various chemical reactions. Its application reason is its ability to participate in carboxylation and esterification processes, which are fundamental in creating a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [2-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate is used as a building block for the synthesis of biologically active compounds. The application reason is its structural properties that allow for the creation of molecules with potential therapeutic effects.
Used in Chemical Research:
[2-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate is also utilized in chemical research as a model compound to study the reactivity and behavior of chloroacetic acid esters in different reaction conditions. The application reason is to gain insights into the underlying mechanisms of these reactions, which can be applied to develop new synthetic methods or improve existing ones.
Used in Chemical Education:
[2-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate can be used in chemical education as an example of a chloroacetic acid ester, illustrating the principles of esterification and the importance of handling such compounds with care. The application reason is to provide students with a practical understanding of the properties and potential hazards associated with this class of compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 4376-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4376-28:
(6*4)+(5*3)+(4*7)+(3*6)+(2*2)+(1*8)=97
97 % 10 = 7
So 4376-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H13ClO3/c17-10-16(19)20-11-15(18)14-8-6-13(7-9-14)12-4-2-1-3-5-12/h1-9H,10-11H2

4376-28-7SDS

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-oxo-2-(4-phenylphenyl)ethyl] 2-chloroacetate

1.2 Other means of identification

Product number -
Other names p-phenylphenacyl chloroacetate

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:4376-28-7 SDS

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