N-Isopropyl-N-phenylbenzamide

Base Information

Chemical Name:N-Isopropyl-N-phenylbenzamide
CAS No.:16466-45-8
Molecular Formula:C₁₆H₁₇NO
Molecular Weight:239.317
Hs Code.:
DSSTox Substance ID:DTXSID501293360
Nikkaji Number:J3.426.875D

Synonyms:N-Isopropyl-N-phenylbenzamide;SCHEMBL1005473;DTXSID501293360;N-(1-methylethyl)-N-phenylbenzamide;AKOS034570920;Z751279908;16466-45-8

Suppliers and Price of N-Isopropyl-N-phenylbenzamide

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
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price

Total 1 raw suppliers

Chemical Property of N-Isopropyl-N-phenylbenzamide

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:239.131014166
Heavy Atom Count:18
Complexity:262

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)N(C1=CC=CC=C1)C(=O)C2=CC=CC=C2

Technology Process of N-Isopropyl-N-phenylbenzamide

There total 5 articles about N-Isopropyl-N-phenylbenzamide 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: 82.0%

: 93-98-1,5705-51-1
N-phenyl benzoyl amide

: 513-02-0
triisopropyl phosphate

: 16466-45-8
N-isopropyl-N-phenylbenzamide

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at 0 - 120 ℃; for 24h; regioselective reaction;
DOI:10.1055/a-1504-8366

Reference yield: 72.0%

: 16466-45-8
N-isopropyl-N-phenylbenzamide

Guidance literature:: With lithium diisopropyl amide; at 0 ℃; for 0.25h;

at 120 ℃; for 24h;

Reference yield: 54.0%

: 10545-45-6
N-isopropyl-N-methylaniline

: 100-52-7
benzaldehyde

: 16466-45-8
N-isopropyl-N-phenylbenzamide

: 1934-92-5
N-methyl-N-phenyl-benzamide

Guidance literature:: With tert.-butylhydroperoxide; iron(II) chloride; In decane; acetonitrile; at 85 ℃; for 1h; chemoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1002/chem.201203824