Piperidine, 1-((2-(phenoxymethyl)cyclopropyl)carbonyl)-4-phenyl-, trans-

Base Information

Chemical Name:Piperidine, 1-((2-(phenoxymethyl)cyclopropyl)carbonyl)-4-phenyl-, trans-
CAS No.:102634-79-7
Molecular Formula:C₂₂H₂₅NO₂
Molecular Weight:335.446
Hs Code.:
DSSTox Substance ID:DTXSID40145424
Wikidata:Q76423308
Mol file:102634-79-7.mol

Synonyms:BRN 5605462;Piperidine, 1-((2-(phenoxymethyl)cyclopropyl)carbonyl)-4-phenyl-, trans-;102634-79-7;trans-1-((2-(Phenoxymethyl)cyclopropyl)carbonyl)-4-phenylpiperidine;DTXSID40145424

Suppliers and Price of Piperidine, 1-((2-(phenoxymethyl)cyclopropyl)carbonyl)-4-phenyl-, trans-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Piperidine, 1-((2-(phenoxymethyl)cyclopropyl)carbonyl)-4-phenyl-, trans-

Chemical Property:

Vapor Pressure:1E-10mmHg at 25°C
Boiling Point:515.3°C at 760 mmHg
Flash Point:265.4°C
Density:1.149g/cm³
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:335.188529040
Heavy Atom Count:25
Complexity:431

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CCC1C2=CC=CC=C2)C(=O)C3CC3COC4=CC=CC=C4
Isomeric SMILES:C1CN(CCC1C2=CC=CC=C2)C(=O)[C@@H]3C[C@H]3COC4=CC=CC=C4

Technology Process of Piperidine, 1-((2-(phenoxymethyl)cyclopropyl)carbonyl)-4-phenyl-, trans-

There total 4 articles about Piperidine, 1-((2-(phenoxymethyl)cyclopropyl)carbonyl)-4-phenyl-, trans- 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: 56.0%

: 771-99-3
4-phenylpiperidine

: 102617-03-8
trans-2-phenoxymethylcyclopropane-1-carbonyl chloride

: 102634-79-7
trans-1-<4-phenylpiperidin-1-ylcarbonyl>-2-phenoxymethylcyclopropane

Guidance literature:: With triethylamine; In benzene; Heating;

Reference yield:

: 122-60-1,71031-02-2
Phenyl glycidyl ether

: 102634-79-7
trans-1-<4-phenylpiperidin-1-ylcarbonyl>-2-phenoxymethylcyclopropane

Guidance literature:: Multi-step reaction with 4 steps

1: 7 g / 8 h / 195 - 200 °C

2: 88 percent / 10 N KOH / ethanol / 28 h / Heating

3: 1.25 g / SOCl₂ / benzene / 4 h / Heating

4: 56 percent / triethylamine / benzene / Heating

With potassium hydroxide; thionyl chloride; triethylamine; In ethanol; benzene;

Reference yield:

: 102617-01-6,102617-02-7,121185-32-8
trans-2-phenoxymethylcyclopropane-1-carboxylic acid

: 102634-79-7
trans-1-<4-phenylpiperidin-1-ylcarbonyl>-2-phenoxymethylcyclopropane

Guidance literature:: Multi-step reaction with 2 steps

1: 1.25 g / SOCl₂ / benzene / 4 h / Heating

2: 56 percent / triethylamine / benzene / Heating

With thionyl chloride; triethylamine; In benzene;