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2-(4-CHLORO-PHENYL)-SUCCINIC ACID is a chemical compound characterized by the molecular formula C10H9ClO4. It is a dicarboxylic acid derivative featuring a 4-chloro-phenyl group attached to the succinic acid backbone. 2-(4-CHLORO-PHENYL)-SUCCINIC ACID is of interest in pharmaceutical and medicinal chemistry due to its unique structural features, which may allow it to serve as a building block for the synthesis of biologically active molecules or as a starting material for the development of new drugs. Its potential extends to the development of new materials and as a reagent in organic synthesis, with the presence of a chloro group in the phenyl ring adding to its research and application value.

58755-91-2

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58755-91-2 Usage

Uses

Used in Pharmaceutical and Medicinal Chemistry:
2-(4-CHLORO-PHENYL)-SUCCINIC ACID is used as a building block for the synthesis of biologically active molecules, leveraging its structural features to create compounds with potential therapeutic effects.
Used in Drug Development:
2-(4-CHLORO-PHENYL)-SUCCINIC ACID serves as a starting material in the development of new drugs, where its unique properties can be harnessed to address specific medical needs or to improve the efficacy and safety of existing medications.
Used in Material Science:
2-(4-CHLORO-PHENYL)-SUCCINIC ACID has the potential to be utilized in the development of new materials, possibly due to its ability to form complexes or participate in polymerization reactions that result in materials with novel properties.
Used as a Reagent in Organic Synthesis:
In the field of organic synthesis, 2-(4-CHLORO-PHENYL)-SUCCINIC ACID is used as a reagent, contributing to the formation of a wide range of organic compounds through various chemical reactions, such as esterification, amidation, or substitution reactions.
Used in Research and Development:
The presence of a chloro group in the phenyl ring makes 2-(4-CHLORO-PHENYL)-SUCCINIC ACID a subject of interest for further research, potentially leading to new discoveries and applications in various scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 58755-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,5 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58755-91:
(7*5)+(6*8)+(5*7)+(4*5)+(3*5)+(2*9)+(1*1)=172
172 % 10 = 2
So 58755-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClO4/c11-7-3-1-6(2-4-7)8(10(14)15)5-9(12)13/h1-4,8H,5H2,(H,12,13)(H,14,15)

58755-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-CHLORO-PHENYL)-SUCCINIC ACID

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

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More Details:58755-91-2 SDS

58755-91-2Relevant academic research and scientific papers

Enamines; 45. A New Simple Synthesis of 2-Phenylsuccinic Acids

Rossi, Elisabetta,Sassano, Silvia,Stradi, Riccardo

, p. 765 - 766 (2007/10/02)

A simple route to 2-phenylsuccinic acids consists of the reaction of 1,1-dimorpholinoethene with β-nitrostyrenes at room temperature and hydrolysis of the 1:1 adduct thus obtained with hydrochloric acid.The method affords good overall yields of 2-phenylsuccinic acids.

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