19344-29-7

Basic information

• Product Name: 3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL
• Synonyms: 3-((2-HYDROXYETHYL)AMINO)PROPANOL;N-Ethanolpropanolamine;3-((2-HYDROXYETHYL)A;3-(2-hydroxyethylaMino)propan-1-ol;B-HYDROXYETHYL-G-HYDROXYPROPYLAMINE;3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL
• CAS NO: 19344-29-7
• Molecular Formula: C₅H₁₃NO₂
• Molecular Weight: 119.16
• EINECS: 242-978-3
• Mol File: 19344-29-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 259.4°Cat760mmHg
• Flash Point: 137.9°C
• Appearance: /
• Density: 1.037g/cm³
• Vapor Pressure: 0.0019mmHg at 25°C
• Refractive Index: 1.466
• CAS DataBase Reference: 3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL(19344-29-7)
• EPA Substance Registry System: 3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL(19344-29-7)

Safety Data

• Hazardous Substances Data: 19344-29-7(Hazardous Substances Data)

Usage

General Description

3-((2-Hydroxyethyl)Amino)-1-Propanol is a chemical compound that belongs to the class of organic compounds known as aminoalcohols, which are alcohols that contain an amino group. It is typically used in a variety of industrial and scientific applications. The hydroxyethyl group and the amino group in the structure make it a dual functional compound. Such compounds are often used as intermediates in organic synthesis due to their reactivity. Moreover, the presence of these functional groups endows the compound with polar properties, which might make it soluble in water and other polar solvents. However, like other chemicals, it should be handled with care as exposure may cause various health risks.

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

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

Relevant articles and documents

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.

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.

Synthesis of hexahydroxazepine-1,4 derivatives with expected pharmacological action. I. Synthesis of N-alkyl-derivatives of hexahydrooxazepine-1,4

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