5350-64-1 Usage
Uses
1. Used in Chemical Synthesis:
4-PYRIDINAMINE, 5-ETHYL-2-METHYLis used as a building block in chemical synthesis for the development of various products. Its unique structure allows it to be a valuable component in the creation of more complex molecules, which can be utilized in different industries.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-PYRIDINAMINE, 5-ETHYL-2-METHYLis used as a key intermediate in the synthesis of various drugs. Its chemical properties make it suitable for the development of new medications, potentially contributing to the treatment of various health conditions.
3. Used in Research and Development:
4-PYRIDINAMINE, 5-ETHYL-2-METHYLis also utilized in research and development for the study of its chemical properties and potential applications. This can lead to the discovery of new uses and advancements in various fields, including materials science, pharmaceuticals, and chemical engineering.
4. Used in Product Contact:
In certain industries, 4-PYRIDINAMINE, 5-ETHYL-2-METHYLmay be used in applications where it comes into contact with products, such as in the manufacturing of specific coatings or additives. Its properties may provide benefits in terms of product performance, durability, or other desired characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 5350-64-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5350-64:
(6*5)+(5*3)+(4*5)+(3*0)+(2*6)+(1*4)=81
81 % 10 = 1
So 5350-64-1 is a valid CAS Registry Number.
5350-64-1Relevant academic research and scientific papers
Improved Synthesis of N1-Pyridylthiamine Pyrophosphate, a Coenzymatically Active Analog of Thiamine Pyrophosphate
Neef, Holger,Golbik, Ralph,Fahlbusch, Baerbel,Schellenberger, Alfred
, p. 913 - 916 (2007/10/02)
Our previously published synthesis of the N1-pyridyl analog 1b of thiamine pyrophosphate is improved resulting in a remarkably higher yield.Key reaction of this new synthetic pathway is the oxidative degradation of 5-acetylpyridine 8 to the 5-carboxylic acid 11 via the pyridinium compound 10.Improved preparations of other intermediates are also described.The N1-pyridylthiamine pyrophosphate analog 1b has been separated and purified by ion exchange chromatography on Sephadex A-25.
