(+-)-1-Amino-1-phenyl-2-undecanone hydrochloride

Base Information

Chemical Name:(+-)-1-Amino-1-phenyl-2-undecanone hydrochloride
CAS No.:153788-02-4
Molecular Formula:C₁₇H₂₇NO*ClH
Molecular Weight:297.868
Hs Code.:
DSSTox Substance ID:DTXSID00934811
ChEMBL ID:CHEMBL1922896

Synonyms:(+-)-1-Amino-1-phenyl-2-undecanone hydrochloride;2-Undecanone, 1-amino-1-phenyl-, hydrochloride, (+-)-;153788-02-4;CHEMBL1922896;DTXSID00934811;LS-158450;1-Amino-1-phenylundecan-2-one--hydrogen chloride (1/1)

Suppliers and Price of (+-)-1-Amino-1-phenyl-2-undecanone hydrochloride

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (+-)-1-Amino-1-phenyl-2-undecanone hydrochloride

Chemical Property:

Vapor Pressure:1.35E-05mmHg at 25°C
Boiling Point:367.6°C at 760 mmHg
Flash Point:176.1°C
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:10
Exact Mass:297.1859422
Heavy Atom Count:20
Complexity:233

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCC(=O)C(C1=CC=CC=C1)N.Cl

Technology Process of (+-)-1-Amino-1-phenyl-2-undecanone hydrochloride

There total 6 articles about (+-)-1-Amino-1-phenyl-2-undecanone hydrochloride 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: 57.0%

: Decanoic acid (2-oxo-1-phenyl-undecyl)-amide

: 153788-02-4
DL-1-Amino-1-phenyl-undecan-2-on-hydrochlorid

Guidance literature:: With hydrogenchloride; In ethanol; for 8h; Heating;

Reference yield: 7.0%

: 1351299-60-9
1-(tert-butoxycarbonylamino)-1-phenylundecan-2-one

: 153788-02-4
DL-1-Amino-1-phenyl-undecan-2-on-hydrochlorid

Guidance literature:: With hydrogenchloride; In diethyl ether; water; Inert atmosphere;
DOI:10.1016/j.bmc.2011.09.021

Reference yield:

: 2900-27-8,3601-66-9,14675-97-9,33125-05-2
2-(tert-butoxycarbonylamino)-2-phenylacetic acid

: 153788-02-4
DL-1-Amino-1-phenyl-undecan-2-on-hydrochlorid

Guidance literature:: Multi-step reaction with 4 steps

1.1: dichloromethane / 0 - 20 °C / Inert atmosphere

2.1: 1H-imidazole; dmap / dichloromethane / 0 - 20 °C / Inert atmosphere

3.1: magnesium / diethyl ether / 20 °C / Inert atmosphere

3.2: 20 °C / Inert atmosphere

3.3: Inert atmosphere

4.1: hydrogenchloride / diethyl ether; water / Inert atmosphere

With 1H-imidazole; hydrogenchloride; dmap; magnesium; In diethyl ether; dichloromethane; water; 3.2: Grignard reaction;
DOI:10.1016/j.bmc.2011.09.021