32599-04-5

Basic information

• Product Name: 1-phenoxy-3-(piperidin-1-yl)propan-2-ol
• Synonyms: 1-phenoxy-3-(1-piperidinyl)-2-propanol; 1-Phenoxy-3-(piperidin-1-yl)propan-2-ol; 1-Phenoxy-3-piperidin-1-yl-propan-2-ol; 1-Piperidineethanol, alpha-(phenoxymethyl)-
• CAS NO: 32599-04-5
• Molecular Formula: C₁₄H₂₁NO₂
• Molecular Weight: 235.322
• Mol File: 32599-04-5.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 386.5°C at 760 mmHg
• Flash Point: 187.5°C
• Density: 1.08g/cm³
• Vapor Pressure: 1.15E-06mmHg at 25°C
• Refractive Index: 1.539
• CAS DataBase Reference: 1-phenoxy-3-(piperidin-1-yl)propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenoxy-3-(piperidin-1-yl)propan-2-ol(32599-04-5)
• EPA Substance Registry System: 1-phenoxy-3-(piperidin-1-yl)propan-2-ol(32599-04-5)

Safety Data

• Hazardous Substances Data: 32599-04-5(Hazardous Substances Data)

Usage

Molecular structure

Consists of a phenoxy group, a piperidin-1-yl group, and a propan-2-ol group.

Usage

Commonly used as an intermediate in the synthesis of pharmaceuticals, fragrances, and other organic compounds.

Potential applications

May be utilized in the development of new drugs for the treatment of various medical conditions.

Aromatic properties

Can be used in the production of flavors and fragrances due to its aromatic nature.

Versatility

Has diverse potential uses in various industries, including medicine, flavor production, and fragrance development.

Upstream product

• 111-24-0 1,5-dibromo-pentane 
• 4287-19-8 1-amino-3-phenoxy-isopropanol 
• 110-89-4 piperidine 
• 122-60-1 Phenyl glycidyl ether 

Downstream Products

• 101256-22-8 acetic acid-(β-phenoxy-β'-piperidino-isopropyl ester) 

Relevant articles and documents

Influence of the structure of polyfluorinated alcohols on Bronsted acidity/hydrogen-bond donor ability and consequences on the promoter effect

The influence of substituents on the properties of tri-and hexafluorinated alcohols derived from 2,2,2-trifluoroethanol (TFE) and 1,1,1,3,3,3-hexafluoro-2- propanol (HFIP) was examined. Measurements of specific solvent-solute interactions revealed that H-

Synthesis of new 3-phenoxypropan-2-ols with various heterocyclic substituents

1-Phenoxy-3-piperidinopropan-2-ol, 1-(5-methyl-1,3-benzothiazol-2- ylsulfanyl)-3-phenoxypropan-2-ol, 1-(2-hydroxy-3-phenoxypropyl)azepan-2-one, 1,1′-(6-chloro-1,3-benzothiazol-2-ylimino)bis(3-phenoxypropan-2-ol), 1-(1,3-benzothiazol-2-ylsulfanyl)-3-phenox

Fe(OH)3 nano solid material: An efficient catalyst for regioselective ring opening of aryloxy epoxide with amines under solvent free condition

Iron hydroxide-Fe(OH)3and iron oxides (Fe3O4and Fe2O3) were successfully prepared and characterized. These materials were employed as efficient and environmentally benign heterogeneous catalysts for t

Phenalenyl in a different role: Catalytic activation through the nonbonding molecular orbital

We have demonstrated that the nonbonding molecular orbital (NBMO) of the phenalenyl (PLY) cation can be used as a Lewis acid catalyst for different organic transformations. Detailed computational and spectroscopic studies for the aminolysis reaction of ep