1-Cinnamoylazepane

Base Information

Chemical Name:1-Cinnamoylazepane
CAS No.:27845-73-4
Molecular Formula:C₁₅H₁₉NO
Molecular Weight:229.322
Hs Code.:
DSSTox Substance ID:DTXSID201195882
ChEMBL ID:CHEMBL2229621

Synonyms:1-cinnamoylazepane;SCHEMBL692605;CHEMBL2229621;DTXSID201195882;STK414157;AKOS002987108;AB00077418-01;SR-01000201775;(2E)-1-(azepan-1-yl)-3-phenylprop-2-en-1-one;SR-01000201775-1;(2E)-1-(Hexahydro-1H-azepin-1-yl)-3-phenyl-2-propen-1-one;27845-73-4

Suppliers and Price of 1-Cinnamoylazepane

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 0 raw suppliers

Chemical Property of 1-Cinnamoylazepane

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:229.146664230
Heavy Atom Count:17
Complexity:258

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCCN(CC1)C(=O)C=CC2=CC=CC=C2
Isomeric SMILES:C1CCCN(CC1)C(=O)/C=C/C2=CC=CC=C2

Technology Process of 1-Cinnamoylazepane

There total 6 articles about 1-Cinnamoylazepane 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%

: 1-(azepan-1-yl)-3-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propan-1-one

: 27845-73-4
(E)-1-(azepan-1-yl)-3-phenylprop-2-en-1-one

Guidance literature:: With potassium tert-butylate; In N,N-dimethyl-formamide; at 40 ℃; for 1.5h; Inert atmosphere;
DOI:10.1021/acs.joc.9b00872

Reference yield: 62.0%

: 5809-41-6
N-acetylhexahydroazepine

: 100-51-6,185532-71-2
benzyl alcohol

: 27845-73-4
(E)-1-(azepan-1-yl)-3-phenylprop-2-en-1-one

: 1-(azepan-1-yl)-3-phenylprop-2-en-1-one

Guidance literature:: With Eosin Y; potassium hydroxide; at 20 ℃; Irradiation;
DOI:10.1039/c8ob02938e

Reference yield: 59.0%

: 91124-99-1
Hexamethyleneiminocarbonylmethylenetriphenylphosphorane

: 51608-60-7
N-(benzylidene)-p-methylbenzenesulfonamide

: 27845-73-4
(E)-1-(azepan-1-yl)-3-phenylprop-2-en-1-one

Guidance literature:: In dimethyl sulfoxide; at 100 ℃; for 12h; optical yield given as %de; stereoselective reaction; Inert atmosphere;
DOI:10.1002/ejoc.201001379