132424-10-3

Basic information

• Product Name: N-methyl-N-(3-phenoxypropyl)amine
• Synonyms: N-methyl-N-(3-phenoxypropyl)amine;N-METHYL-3-PHENOXY-1-PROPANAMINE;N-methyl-3-phenoxy-1-propanamine(SALTDATA: FREE);N-Methyl-3-phenoxypropan-1-aMine
• CAS NO: 132424-10-3
• Molecular Formula: C₁₀H₁₅NO
• Molecular Weight: 165.23
• Mol File: 132424-10-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 261.362°C at 760 mmHg
• Flash Point: 103.133°C
• Appearance: /
• Density: 0.962g/cm³
• Vapor Pressure: 0.012mmHg at 25°C
• Refractive Index: 1.499
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N-methyl-N-(3-phenoxypropyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-N-(3-phenoxypropyl)amine(132424-10-3)
• EPA Substance Registry System: N-methyl-N-(3-phenoxypropyl)amine(132424-10-3)

Safety Data

• Hazardous Substances Data: 132424-10-3(Hazardous Substances Data)

Usage

General Description

N-methyl-N-(3-phenoxypropyl)amine is an organic compound with the chemical formula C11H17NO. It is a tertiary amine, with a methyl group and a phenoxypropyl group attached to the nitrogen atom. N-methyl-N-(3-phenoxypropyl)amine is commonly used as a reactant in organic syntheses and as a building block for the synthesis of various chemical compounds. It is known for its role in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. N-methyl-N-(3-phenoxypropyl)amine is a clear, colorless liquid with a strong, ammonia-like odor, and it is considered to be a hazardous substance, requiring careful handling and storage.

InChI:InChI=1/C10H15NO/c1-11-8-5-9-12-10-6-3-2-4-7-10/h2-4,6-7,11H,5,8-9H2,1H3

Upstream product

• 588-63-6 3-phenoxypropyl bromide 
• 74-89-5 methylamine 
• 108-95-2 phenol 

Downstream Products

• 228567-52-0 11β-fluoro-7α-{5-[methyl-(3-phenoxy-propyl)-amino]-pentyl}-estra-1,3,5(10)-triene-3,17β-diol 
• 1146681-11-9 2-(2,4-difluorophenyl)-3-[methyl-(3-phenoxypropyl)amino]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol 

Relevant articles and documents

Synthesis of Medium-Ring-Sized Benzolactams by Using Strong Electrophiles and Quantitative Evaluation of Ring-Size Dependency of the Cyclization Reaction Rate

Benzolactams with medium-sized rings were synthesized via the electrophilic aromatic substitution reaction of carbamoyl cations (R1R2N+═C═O) in good to high yields without dilution. These reactions were utilized to quantitatively examine the extent of retardation of medium-sized ring formation, compared to five- or six-membered ring formation. The order of reaction rates of formation of cyclic benzolactams is six- > five- > seven- > eight- > nine-membered ring at 25 °C. The present reaction provides a route to eight- A nd nine-membered benzolactams.

11BETA-HALOGEN-7ALPHA-SUBSTITUTED ESTRATRIENES, METOD FOR PRODUCING PHARMACEUTICAL PREPARATIONS CONTAINING SAID 11BETA-HALOGEN-7ALPHA- SUBSTITUTED ESTRATRIENES AND USE OF THE SAME FOR PRODUCING MEDICAMENTS

This invention describes the new 11β-halogen-7α-substituted estratrienes of general formula I in which R11 is a fluorine or chlorine atom, and the other substituents have the meanings that are explained in more detail in the description. The compounds have antiestrogenic properties or tissue-selective estrogenic properties and are suitable for the production of pharmaceutical agents.