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2,2-diphenylpropanedioic acid, commonly known as benzilic acid, is a white crystalline solid with the chemical formula C14H12O4. It is a member of the diphenylpropanoic acid class and is characterized by its unique molecular structure, featuring two phenyl groups attached to a central carbon atom. This structure endows it with carboxylic acid groups, making it a versatile reagent for a range of organic reactions, including esterification and amidation. Additionally, its distinctive properties make it an important tool in the study of stereochemistry and asymmetric synthesis.

5457-11-4

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5457-11-4 Usage

Uses

Used in Pharmaceutical Industry:
2,2-diphenylpropanedioic acid is used as an intermediate in the synthesis of various pharmaceuticals. Its carboxylic acid groups facilitate the formation of esters and amides, which are essential in the construction of complex drug molecules. This makes it a valuable component in the development of new medications and the improvement of existing ones.
Used in Dye Industry:
2,2-diphenylpropanedioic acid is used as a starting material in the production of dyes. Its phenyl groups and carboxylic acid functionality contribute to the formation of chromophores, which are responsible for the color properties of dyes. This makes it an essential component in the creation of a wide array of dyes for various applications, including textiles, plastics, and printing inks.
Used in Organic Synthesis:
2,2-diphenylpropanedioic acid is used as a reagent in various organic reactions. Its carboxylic acid groups make it a useful agent for esterification and amidation, which are fundamental reactions in the synthesis of a multitude of organic compounds. This versatility allows it to be employed in the preparation of a broad spectrum of chemical products, from simple esters to complex natural products and pharmaceuticals.
Used in Stereochemistry and Asymmetric Synthesis Research:
2,2-diphenylpropanedioic acid is used as a model compound in the study of stereochemistry and asymmetric synthesis. Its unique molecular structure, with two phenyl groups and a central carbon atom, provides a platform for investigating the effects of stereochemistry on reaction outcomes and the development of enantioselective synthetic methods. This makes it an important tool for researchers in the field of organic chemistry, particularly those focused on asymmetric synthesis and the creation of chiral molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 5457-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5457-11:
(6*5)+(5*4)+(4*5)+(3*7)+(2*1)+(1*1)=94
94 % 10 = 4
So 5457-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O4/c16-13(17)15(14(18)19,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H,16,17)(H,18,19)

5457-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diphenylpropanedioic acid

1.2 Other means of identification

Product number -
Other names diphenylpropanedioic acid

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:5457-11-4 SDS

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