3517-23-5 Usage
Uses
Used in Organic Chemistry:
4-[(E)-phenyldiazenyl]phenylacetic acid is utilized as an intermediate in the synthesis of azo dyes, which are essential for various applications, including the coloring of fabrics, plastics, and other materials. Its presence in the synthesis process is crucial for the development of dyes with specific color characteristics and properties.
Used in Materials Science:
In the field of materials science, 4-[(E)-phenyldiazenyl]phenylacetic acid is employed as a building block for the creation of novel materials with tailored properties. Its unique structure allows for the development of materials with enhanced characteristics, such as improved stability, reactivity, or specific interactions with other molecules.
Used in Chemical Processes:
4-[(E)-phenyldiazenyl]phenylacetic acid's reactivity and properties make it a valuable asset in various chemical processes. It can be used as a catalyst or a reactant in the production of other chemicals, contributing to the efficiency and effectiveness of these processes.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the compound's potential applications in the pharmaceutical industry could include its use in the development of new drugs or drug delivery systems, given its unique structure and reactivity. Further research and development would be necessary to explore these possibilities fully.
Check Digit Verification of cas no
The CAS Registry Mumber 3517-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3517-23:
(6*3)+(5*5)+(4*1)+(3*7)+(2*2)+(1*3)=75
75 % 10 = 5
So 3517-23-5 is a valid CAS Registry Number.
3517-23-5Relevant academic research and scientific papers
Development of Peptide-Based Sirtuin Defatty-Acylase Inhibitors Identified by the Fluorescence Probe, SFP3, That Can Efficiently Measure Defatty-Acylase Activity of Sirtuin
Kawaguchi, Mitsuyasu,Ieda, Naoya,Nakagawa, Hidehiko
, p. 5434 - 5452 (2019/06/17)
Sirtuins (SIRTs) are a family of nicotinamide adenine dinucleotide-dependent histone deacetylases that serve as epigenetic regulators of many physiological processes. Recent studies have shown that in addition to their well-known deacetylase activity, sir
The Electronic Effect of the Phenylazo and t-Butylazo Groups
Byrne, Christopher J.,Happer, Duncan A. R.,Hartshorn, Michael P.,Powell, H. Kipton J.
, p. 1649 - 1654 (2007/10/02)
Hammett ?p+-values for arylazo and t-butylazo groups have been determined by measurements of the kinetics of solvolysis of the appropriately substituted arylpropan-2-yl chlorides.They have been found to be considerably more positive than expected and differ significantly from earlier estimates based on the rates of electrophilic attack on azobenzene.An interpretation of the discrepancy has been advanced based on the differing orientations of the azo linkage with respect to the aromatic ring in the transition state.The introduction of methyl groups into positions ortho to the phenylazo and t-butylazo substituents causes a change in character from -I, -R to -I, +R.This is true not only for the solvolysis reaction but also for benzoic acid ionisation.
