41510-06-9

Basic information

• Product Name: 1-(morpholin-4-yl)-3-(naphthalen-1-yloxy)propan-2-ol
• Synonyms: 1-(4-morpholinyl)-3-(1-naphthyloxy)-2-propanol; 1-(Morpholin-4-yl)-3-(1-naphthyloxy)propan-2-ol; 1-Morpholin-4-yl-3-(naphthalen-1-yloxy)propan-2-ol; 1-Morpholin-4-yl-3-(naphthalen-1-yloxy)-propan-2-ol; 4-morpholineethanol, alpha-[(1-naphthalenyloxy)methyl]-
• CAS NO: 41510-06-9
• Molecular Formula: C₁₇H₂₁NO₃
• Molecular Weight: 287.3535
• Mol File: 41510-06-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 491.7°C at 760 mmHg
• Flash Point: 251.2°C
• Density: 1.182g/cm³
• Vapor Pressure: 1.74E-10mmHg at 25°C
• Refractive Index: 1.6
• CAS DataBase Reference: 1-(morpholin-4-yl)-3-(naphthalen-1-yloxy)propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(morpholin-4-yl)-3-(naphthalen-1-yloxy)propan-2-ol(41510-06-9)
• EPA Substance Registry System: 1-(morpholin-4-yl)-3-(naphthalen-1-yloxy)propan-2-ol(41510-06-9)

Safety Data

• Hazardous Substances Data: 41510-06-9(Hazardous Substances Data)

Usage

Chemical structure

The compound has a unique structure that includes a morpholine ring, a naphthalene group, and a propan-2-ol moiety.

Biological activity

The morpholine ring provides biological activity to the compound.

Research tool

It is commonly used as a research tool in the field of organic chemistry.

Intermediate in synthesis

The compound is used as an intermediate in the synthesis of pharmaceuticals and other organic compounds.

Potential applications

It has potential applications in the development of new drugs and bioactive molecules due to its structural diversity and pharmacological properties.

Further research needed

More research is required to fully understand the potential uses and effects of 1-(morpholin-4-yl)-3-(naphthalen-1-yloxy)propan-2-ol.

Upstream product

• 110-91-8 morpholine 
• 2461-42-9 3-(1-naphthyloxy)-1,2-epoxypropane 
• 90-15-3 α-naphthol 

Downstream Products

• 105996-50-7 4-Allyl-4-[2-hydroxy-3-(naphthalen-1-yloxy)-propyl]-morpholin-4-ium; bromide 

Relevant articles and documents

Glycerine and CeClH: An efficient and recyclable reaction medium for ring opening of epoxides with thioamides and amines

Oxiranes undergo rapid ring-opening reaction with a range of thioamides and amines to afford the corresponding -amino alcohol derivatives. The reactions were carried out using glycerine and cerium(III) chloride as a recyclable reaction medium. All the reactions were carried out at room temperature and the products were obtained in excellent yields. Georg Thieme Verlag Stuttgart New York.

Aryloxy propyldiamines

Disclosed herein are compounds of the formula STR1 in which Ar is l-naphthyl; R1 and R2 are either the same or different selected from the group consisting of hydrogen or lower alkyl, or R1 and R2 together with the nitrogen atom to which they are joined form a heterocyclic amine radical selected from the group consisting of 1-pyrrolidinyl, piperidine, morpholine and 4-(lower alkyl)-1-piperazinyl; and R3 and R4 are either the same or different selected from the group consisting of hydrogen or lower alkyl, or R3 and R4 together with the nitrogen to which they are joined represent a heterocyclic amine radical selected from the group consisting of 1-pyrrolidinyl, piperidino, morpholino and 4-(lower alkyl)-1-piperazinyl; or a therapeutically acceptable acid addition salt thereof. The compounds are antidepressant agents and methods for their preparation and use also are disclosed.