138650-06-3 Usage
Uses
Used in Dye and Pigment Manufacturing:
2,3-Pyridinediamine, 6-ethoxyis used as a key intermediate in the production of dyes and pigments for various applications, including textiles, plastics, and printing inks. Its reactivity allows for the creation of a wide range of colorants with different properties.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,3-Pyridinediamine, 6-ethoxyserves as a building block for the synthesis of various drugs. Its unique chemical structure contributes to the development of new medicinal compounds with potential therapeutic effects.
Used in Hair Dye Formulation:
Leveraging its oxidative properties, 2,3-Pyridinediamine, 6-ethoxyis used in the formulation of hair dyes. It helps in the coloration process, providing a range of shades and enhancing the durability of the color.
Used in Organic Synthesis:
2,3-Pyridinediamine, 6-ethoxyis utilized in organic synthesis for the preparation of complex organic molecules. Its ability to form various chemical bonds makes it a valuable component in the synthesis of specialty chemicals and advanced materials.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,3-Pyridinediamine, 6-ethoxyis studied for its potential applications in the development of new drugs and therapeutic agents. Its unique structure and reactivity offer opportunities for the design of novel pharmaceutical compounds with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 138650-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138650-06:
(8*1)+(7*3)+(6*8)+(5*6)+(4*5)+(3*0)+(2*0)+(1*6)=133
133 % 10 = 3
So 138650-06-3 is a valid CAS Registry Number.
138650-06-3Relevant academic research and scientific papers
Diaminopyridine compounds and methods of use
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, (2008/06/13)
The present invention relates to compositions and method for inhibiting nonenzymatic cross-linking (protein aging) which contain diaminopyridines and derivates thereof. Accordingly, a composition is disclosed which comprises an agent capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation. The method comprises contacting the target protein with the composition. Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.
A new route to 6-substituted 2,3-diaminopyridines
Bussolotti,LaMattina,James
, p. 6503 - 6506 (2007/10/02)
2,3-Diaminopyridine reacts with cyclohexanone to form dihydro-4-azabenzimidazole-2-spirocyclohexane. Reaction of this intermediate with a variety of nucleophiles (e.g., water, phenylmercaptan, ethanol, dimethylamine, and diethylmalonate) in the presence o
