4379-15-1 Usage
Uses
Used in Pharmaceutical Industry:
3-AMINO-4-METHYL-PENTAN-1-OL is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines. Its unique chemical structure allows it to be a key component in creating molecules with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-AMINO-4-METHYL-PENTAN-1-OL serves as an intermediate for the production of agrochemicals, which are essential in agriculture for pest control, weed management, and crop protection, thereby ensuring increased crop yields and food security.
Used in Surfactant and Detergent Production:
3-AMINO-4-METHYL-PENTAN-1-OL is employed in the manufacturing process of surfactants and detergents, which are crucial for their effectiveness in cleaning and emulsifying applications across various industries, including consumer goods, textiles, and industrial cleaning.
Used in Lubricant Industry:
3-AMINO-4-METHYL-PENTAN-1-OL is also used in the formulation of lubricants, enhancing their performance by improving properties such as viscosity, reducing friction, and providing protection against wear and tear in various mechanical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4379-15-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4379-15:
(6*4)+(5*3)+(4*7)+(3*9)+(2*1)+(1*5)=101
101 % 10 = 1
So 4379-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO/c1-5(2)6(7)3-4-8/h5-6,8H,3-4,7H2,1-2H3
4379-15-1Relevant academic research and scientific papers
Substituent effects in the ring-chain tautomerism of 4-alkyl-2-aryl substituted oxazolidines and tetrahydro-1,3-oxazines
Juhasz, Marta,Lazar, Laszlo,Fueloep, Ferenc
, p. 1465 - 1473 (2008/09/18)
(Chemical Equation Presented) The condensation products of 2-aminoethanol or 3-aminopropanol (bearing an alkyl substituent on the carbon adjacent to the nitrogen) with substituted benzaldehydes proved to exist in CDCl3 at 300 K as three-component tautomeric mixtures of the diastereomeric five- or six-membered 1,3-O,N-heterocyclic ring forms and the corresponding imines. For each equilibrium, the electronic effects of the 2-aryl substituents were characterized by the Hammett equation. The steric effects of the alkyl groups could be described by Hansch-type equations for the equilibria involving oxazolidine ring forms. While the alkyl substituents did not cause any significant effect on the ring cis-chain and the ring trans-chain equilibria for tetrahydro-1,3-oxazines, increasing bulk of the 4-alkyl group increased the stability of the cyclic tautomers for the analogous oxazolidines.
