4379-15-1 Usage
General Description
3-AMINO-4-METHYL-PENTAN-1-OL, also known as 3-amino-4-methyl-1-pentanol, is an organic compound with the molecular formula C6H15NO. It is a clear, colorless liquid with a slight amine odor. This chemical compound is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used in the production of surfactants, detergents, and lubricants. 3-AMINO-4-METHYL-PENTAN-1-OL is a versatile compound with various applications in the chemical industry and is considered to be a valuable building block for the synthesis of many other organic compounds.
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 articles and documents
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.
