95627-01-3 Usage
Description
4,4’-(Ethylenediimino)dibenzoic Acid, also known as N,N'-diarylethylenediamine derivative, is a chemical compound that serves as a model for tetrahydrofolic acid in nonenzymic reactions. It is characterized by its ethylenediimino linkage and dibenzoic acid structure, which contribute to its unique chemical properties and potential applications.
Uses
Used in Chemical Research:
4,4’-(Ethylenediimino)dibenzoic Acid is used as a model compound for tetrahydrofolic acid in nonenzymic reactions, allowing researchers to study the chemical behavior and interactions of tetrahydrofolic acid in various experimental conditions. This helps in understanding the underlying mechanisms and potential applications of tetrahydrofolic acid in different fields.
Used in Pharmaceutical Development:
As a model for tetrahydrofolic acid, 4,4’-(Ethylenediimino)dibenzoic Acid can be used in the development of new pharmaceutical compounds and therapies. By studying its properties and interactions in nonenzymic reactions, researchers can gain insights into the design and synthesis of drugs that target specific biological pathways or enzymes related to tetrahydrofolic acid.
Used in Biochemical Analysis:
4,4’-(Ethylenediimino)dibenzoic Acid can be employed in biochemical analysis to investigate the role of tetrahydrofolic acid in various biological processes. This can help in understanding the importance of tetrahydrofolic acid in maintaining cellular functions and its potential as a therapeutic target for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 95627-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,2 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95627-01:
(7*9)+(6*5)+(5*6)+(4*2)+(3*7)+(2*0)+(1*1)=153
153 % 10 = 3
So 95627-01-3 is a valid CAS Registry Number.
95627-01-3Relevant articles and documents
Catalyst-Free Synthesis of Aryl Diamines via a Three-Step Reaction Process
Bulut, Safak,Queen, Wendy L.
, p. 3806 - 3818 (2018/04/14)
The formation of C-N bonds with aryl amines is one of the most widely studied reactions in organic chemistry. Despite this, it is still highly challenging, often requiring expensive, precious metal-based catalysts. Here we report an easy catalyst-free methodology for constructing C-N bonds. The method, which proceeds via the in situ formation of closed ring amidinium ions, allows the preparation of a series of symmetrical and/or unsymmetrical aryl diamines in notably high yields (82-98%) and purity and with a variety of different substituents. The methodology is shown successful for the preparation of aryl diamines having para- and/or meta-substituted carboxyl, nitro, bromo, methoxy, or methyl groups. This green synthetic pathway, which is catalyst free, requires only three steps, and proceeds without the need for purification. Further, it is a new sustainable, economically viable method to achieve an otherwise challenging bond formation.
