4-(Diphenylmethoxy)piperidinium chloride

Base Information

• Chemical Name: 4-(Diphenylmethoxy)piperidinium chloride
• CAS No.: 65214-86-0
• Molecular Formula: C18H21 N O . Cl H
• Molecular Weight: 303.832
• European Community (EC) Number: 265-637-0
• Mol file: 65214-86-0.mol

Synonyms:4-(Diphenylmethoxy)piperidinium chloride;AKOS025295596

Chemical Property of 4-(Diphenylmethoxy)piperidinium chloride

Chemical Property:

• Vapor Pressure: 4.38E-06mmHg at 25°C
• Boiling Point: 383.5°C at 760 mmHg
• Flash Point: 162.9°C
• PSA: 21.26000
• LogP: 4.67540
• Storage Temp.: Inert atmosphere,Room Temperature
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 303.1389920
• Heavy Atom Count: 21
• Complexity: 245

Purity/Quality:

97% ^*data from raw suppliers

4-Diphenylmethoxypiperidinehydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C[NH2+]CCC1OC(C2=CC=CC=C2)C3=CC=CC=C3.[Cl-]
• Use Description: 4-(Diphenylmethoxy)piperidinium chloride is a chemical compound with applications in various fields. In the field of organic chemistry, it can be employed as a reactant or intermediate in the synthesis of complex organic molecules, contributing to the production of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure allows chemists to introduce specific functional groups and structural motifs into target molecules. In the pharmaceutical industry, this compound may play a role as an intermediate in the synthesis of drug candidates or as an ingredient in pharmaceutical formulations. Additionally, in the field of materials science, it may find use as a building block for the creation of specialized polymers or materials with specific properties, aiding in the development of innovative materials for various applications. Its significance varies within these fields, but it consistently plays a pivotal role in advancing chemical synthesis, drug development, and materials innovation across diverse scientific and industrial applications.

Technology Process of 4-(Diphenylmethoxy)piperidinium chloride

There total 2 articles about 4-(Diphenylmethoxy)piperidinium chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

isopropyl alcohol (67-63-0,8013-70-5) + ethyl 4-(diphenylmethoxy)-1-piperidinecarboxylate (65214-84-8) → 4-(diphenylmethoxy)piperidine hydrochloride (65214-86-0)

Guidance literature:

With potassium hydroxide; In water; acetone;

Reference yield:

→ 4-(diphenylmethoxy)piperidine hydrochloride (65214-86-0)

Guidance literature:

Reference yield: 70.0%

4-chloro-1-[4-(1,1-dimethyl-2-oxo-2-pyrrolidin-1-yl-ethyl)-phenyl]-butan-1-one (169280-18-6) + 4-(diphenylmethoxy)piperidine hydrochloride (65214-86-0) → 1-[4-(1,1-Dimethyl-2-oxo-2-pyrrolidin-1-yl-ethyl)-phenyl]-4-[4-(hydroxy-diphenylmethyl)-piperidine-1-yl]butan-1-one

Guidance literature:

With potassium carbonate; In water; xylene; at 100 ℃; for 24h;

upstream raw materials:

isopropyl alcohol

ethyl 4-(diphenylmethoxy)-1-piperidinecarboxylate

Downstream raw materials:

4-[4-[4-(Hydroxydiphenylmethyl-)-1-piperidinyl]-1-oxobutyl]-α,α-dimethylbenzeneacetic acid ethyl ester

ebastine