19344-29-7

Usage

Uses

Used in Organic Synthesis:
3-((2-Hydroxyethyl)Amino)-1-Propanol is used as an intermediate in organic synthesis for its reactivity due to the presence of hydroxyethyl and amino groups.
Used in Pharmaceutical Industry:
3-((2-Hydroxyethyl)Amino)-1-Propanol is used as a building block in the development of pharmaceutical compounds, leveraging its dual functional nature to create complex molecules.
Used in Solvent Systems:
3-((2-Hydroxyethyl)Amino)-1-Propanol is used as a solvent or co-solvent in various chemical processes, taking advantage of its polar properties to dissolve a wide range of substances.
Used in Research Applications:
3-((2-Hydroxyethyl)Amino)-1-Propanol is used in scientific research as a reagent or for the preparation of other compounds, contributing to the advancement of chemical knowledge and innovation.

InChI:InChI=1/C5H13NO2/c7-4-1-2-6-3-5-8/h6-8H,1-5H2

Upstream product

• 75-21-8 oxirane 
• 156-87-6 propan-1-ol-3-amine 

Downstream Products

• 42453-19-0 N-<2-Chlor-ethyl>-3-chlor-propylamin 
• 6965-77-1 N-(2-hydroxyethyl)-N-(3-hydroxypropyl)-para-toluenesulfonamide 
• 121335-74-8 7-tosylperhydro-1,3,6-dioxazonine 
• 23207-87-6 N-<2-Chlor-aethyl>-N-<3-chlor-propyl>-benzylamin 
• 183727-94-8 N-(2-hydroxyethyl)-N-tritylsulfenyl-3-amino-1-propanol 
• 1098091-57-6 N-(2-p-Toluenesulfonylethyl)-N-tritylsulfenyl-3-amino-1-O-p-toluenesulfonylpropanol 

Relevant academic research and scientific papers

Compounds having a plurality of nitrogenous substitutents

Novel compounds having the formula: STR1wherein the constituent variables are defined herein. The compounds are constructed to include a central aromatic, aliphatic, or heterocyclic ring system. Attached to the central ring system are two linear groups having nitrogenous moieties that are derivatized with chemical functional groups. The ring system can include further nitrogenous moieties, either as ring atoms or on pendant groups attached to the ring, that may also be derivatized with chemical functional groups. The totality of the chemical functional groups imparts certain conformational and other properties to the these compounds. In accordance with certain embodiments of the invention, libraries of such compounds are prepared utilizing permutations and combinations of the chemical functional groups and the nitrogenous moieties to build complexity into the libraries.

SUBSTITUTED HETEROCYCLIC COMPOUNDS

Novel compounds having the formula: STR1 wherein the constituent variables are defined herein. The compounds are constructed to include a central aromatic, aliphatic, or heterocyclic ring system. Attached to the central ring system are two linear groups having nitrogenous moieties that are derivatized with chemical functional groups. The ring system can include further nitrogenous moieties, either as ring atoms or on pendant groups attached to the ring, that may also be derivatized with chemical functional groups. The totality of the chemical functional groups imparts certain conformational and other properties to the these compounds. In accordance with certain embodiments of the invention, libraries of such compounds are prepared utilizing permutations and combinations of the chemical functional groups and the nitrogenous moieties to build complexity into the libraries.

Nitrogenous macrocyclic compounds

PCT No. PCT/US96/04215 Sec. 371 Date Sep. 19, 1997 Sec. 102(e) Date Sep. 19, 1997 PCT Filed Mar. 27, 1996 PCT Pub. No. WO96/30377 PCT Pub. Date Oct. 3, 1996Novel macrocyclic compounds are constructed to include large cyclic structures that are interrupted by at least one ring system. Each interrupting ring system includes two bridgehead atoms. Bridgehead atoms are bonded to one or more bridges that interconnect one or more ring systems thereby forming a large cyclic structure. Located in each bridge are two or more nitrogenous moieties that are derivatized with chemical functional groups. The ring systems can include further nitrogenous moieties, either as ring atoms or on pendant groups attached to the ring. These can also be derivatized with chemical functional groups. The totality of the chemical functional groups imparts certain conformational and other properties to the macrocyclic compounds. In accordance with certain embodiments of the invention, libraries of such macrocyclic compounds are prepared utilizing permutations and combinations of the chemical functional groups and the nitrogenous moieties to build complexity into the library.

Candida antarctica Lipase-Catalyzed Monoaminolysis of Diesters with Aminoalcohols. Chemoenzymatic Synthesis of Macrocycles and Aminodiols

Candida antarctica lipase catalyzes the selective monoaminolysis of diesters using aminoalcohols as nucleophiles.The reduction of the amidoseters obtained is a way to prepare symmetrical and unsymmetrical aminodiols.Macrocyclic compounds were isolated in the lipase-catalyzed reactions between dimethyl adipate and 5-amino-1-pentanol and 6-amino-1-hexanol.