2683-57-0 Usage
Uses
Used in Pharmaceutical Synthesis:
5-(Diethylamino)pentyl alcohol is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure allows it to be a versatile building block in the development of new drugs and medications.
Used in Chemical Industry:
In the chemical industry, 5-(Diethylamino)pentyl alcohol is utilized as a reagent or catalyst in various chemical reactions. Its ability to form hydrogen bonds and its solubility in water make it suitable for a wide range of applications, including the production of other organic chemicals.
Used in Research and Development:
5-(Diethylamino)pentyl alcohol is also used in research and development settings to explore its potential applications and properties. Scientists and researchers use it to study its interactions with other compounds and to develop new methods for synthesizing complex organic molecules.
Used in Solvent Applications:
Due to its solubility in water and other solvents, 5-(Diethylamino)pentyl alcohol can be used as a solvent in various industrial processes. It can help dissolve other substances, facilitating chemical reactions and improving the efficiency of certain manufacturing processes.
Used in Specialty Chemicals Production:
5-(Diethylamino)pentyl alcohol is employed in the production of specialty chemicals, such as surfactants, emulsifiers, and other additives. Its unique properties make it valuable in creating customized solutions for specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2683-57-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2683-57:
(6*2)+(5*6)+(4*8)+(3*3)+(2*5)+(1*7)=100
100 % 10 = 0
So 2683-57-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H21NO/c1-3-10(4-2)8-6-5-7-9-11/h11H,3-9H2,1-2H3
2683-57-0Relevant academic research and scientific papers
ETUDE DES INTERACTIONS ENTRE FONCTIONS ALCOOL ET AMINE: EVOLUTION THERMIQUE D'HYDROXYDES ET DE SELS D'ω-TRIALKYLAMMONIO ALCANOLS-1
Barbry, Didier,Hasiak, Bruno
, p. 1734 - 1744 (2007/10/02)
The thermolysis of ω-hydroxyalkyltrialkylammonium hydroxides (Φ=4-8) was investigated: Elimination to alkenol competes with substitution to amino alcohol; the hydroxy group can be alkylated into aliphatic ethers by an intermolecular process; the intramolecular cyclization into cyclic ethers is important only when ω=4.Substitution reaction in amino alcohols is the main pathway for the thermolysis of ω-hydroxyalkyltrimethylammonium acetates (ω=5,6) and chloride (ω=6).
