5-Benzoyl-5H-dibenz[b,f]azepin

Base Information

Chemical Name:5-Benzoyl-5H-dibenz[b,f]azepin
CAS No.:41216-97-1
Molecular Formula:C₂₁H₁₅NO
Molecular Weight:297.356
Hs Code.:
DSSTox Substance ID:DTXSID701275203
Nikkaji Number:J2.010.945I
ChEMBL ID:CHEMBL3103398

Synonyms:CHEMBL3103398;41216-97-1;5-Benzoyl-5H-dibenz[b,f]azepin;Oprea1_233880;Oprea1_564516;SCHEMBL16131284;DTXSID701275203;5-Benzoyl-5H-dibenzo[b,f]azepine;BDBM50446081;STL361143;5-Benzoyl-5H-dibenzo[b,f]azepine #;AKOS000645295;CCG-274872;5H-Dibenz[b,f]azepin-5-ylphenylmethanone;5H-dibenzo[b,f]azepin-5-yl(phenyl)methanone;EN300-26867217;Z62502950;2-benzoyl-2-azatricyclo[9.4.0.0,3,8]pentadeca-1(11),3(8),4,6,9,12,14-heptaene

Suppliers and Price of 5-Benzoyl-5H-dibenz[b,f]azepin

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 5-Benzoyl-5H-dibenz[b,f]azepin

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:297.115364102
Heavy Atom Count:23
Complexity:425

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)N2C3=CC=CC=C3C=CC4=CC=CC=C42

Technology Process of 5-Benzoyl-5H-dibenz[b,f]azepin

There total 1 articles about 5-Benzoyl-5H-dibenz[b,f]azepin 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:

: 256-96-2
dibenzoazepine

: 591-50-4
iodobenzene

: 201230-82-2
carbon monoxide

: 41216-97-1
(5H-dibenzo[b,f]azepin-5-yl)(phenyl)methanone

Guidance literature:: With bis(tri-t-butylphosphine)palladium⁽⁰⁾; tetrabutyl-ammonium chloride; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 65 ℃; for 20h; under 1535.79 Torr; Schlenk technique; Inert atmosphere;
DOI:10.1021/ja4098093