10575-26-5 Usage
Uses
Used in Organic Synthesis:
5-(diethylamino)pent-3-yn-2-ol is used as a building block in organic synthesis for the creation of a variety of pharmaceuticals and biologically active molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of complex organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-(diethylamino)pent-3-yn-2-ol is employed as a key intermediate in the development of new drugs and therapeutic agents. Its presence in the molecular structure can influence the pharmacological properties of the final product, contributing to the discovery of novel treatments for various diseases.
Used in Drug Development:
5-(diethylamino)pent-3-yn-2-ol is utilized in drug development as a potential candidate for the creation of new therapeutic agents. Its unique chemical properties and reactivity make it a promising starting point for the design of innovative pharmaceuticals with improved efficacy and safety profiles.
Used in Research and Development:
5-(diethylamino)pent-3-yn-2-ol is also used in research and development settings to explore its potential applications and to understand its chemical behavior. Studies on 5-(diethylamino)pent-3-yn-2-ol can lead to advancements in the fields of chemistry and medicine, potentially uncovering new uses and applications for this versatile compound.
Check Digit Verification of cas no
The CAS Registry Mumber 10575-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10575-26:
(7*1)+(6*0)+(5*5)+(4*7)+(3*5)+(2*2)+(1*6)=85
85 % 10 = 5
So 10575-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO/c1-4-10(5-2)8-6-7-9(3)11/h9,11H,4-5,8H2,1-3H3
10575-26-5Relevant academic research and scientific papers
Manufacture of 1-disubstituted aminoalk-2-yn-4-ols
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, (2008/06/13)
The manufacture of N-disubstituted 1-aminoalk-2-yn-4-ols by reacting a secondary amine, e.g. a dialkylamine, formaldehyde and an acetylene-alcohol by a Mannich reaction, using a copper catalyst, takes place with better yield and at a higher rate if carried out in the presence of iodine or of a bromide or iodide.
