dibenzo[c,e]oxepin-5(7H)-one

Base Information

Chemical Name:dibenzo[c,e]oxepin-5(7H)-one
CAS No.:4445-34-5
Molecular Formula:C14H10 O2
Molecular Weight:210.232
Hs Code.:2932999099
DSSTox Substance ID:DTXSID20404889
Nikkaji Number:J1.454.898J
Mol file:4445-34-5.mol

Synonyms:dibenzo[c,e]oxepin-5(7H)-one;4445-34-5;Dibenz(c,e)oxepine-5(7H)-one;7H-benzo[d][2]benzoxepin-5-one;Dibenz[c,e]oxepin-5(7H)-one;7H-dibenzo[c,e]oxepin-5-one;SCHEMBL2208963;DTXSID20404889;UYCIYTZGOBZBME-UHFFFAOYSA-N;5H-benzo[d][2]benzoxepin-7-one;MFCD00114923;AKOS000276674;BS-28798

Suppliers and Price of dibenzo[c,e]oxepin-5(7H)-one

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

TRC
Dibenz(c,e)oxepine-5(7H)-one
100mg
$ 105.00

Crysdot
Dibenzo[c,e]oxepin-5(7H)-one 95+%
1g
$ 353.00

American Custom Chemicals Corporation
DIBENZ(C,E)OXEPIN-5(7H)-ONE 95.00%
5MG
$ 495.47

Alichem
Dibenzo[c,e]oxepin-5(7H)-one
1g
$ 400.00

AK Scientific
Dibenzo[c,e]oxepin-5(7H)-one
250mg
$ 284.00

AK Scientific
Dibenzo[c,e]oxepin-5(7H)-one
100mg
$ 168.00

Total 7 raw suppliers

Chemical Property of dibenzo[c,e]oxepin-5(7H)-one

Chemical Property:

PSA：26.30000
LogP:3.02400
Storage Temp.:2-8°C
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:210.068079557
Heavy Atom Count:16
Complexity:274

Purity/Quality:

98%Min ^*data from raw suppliers

Dibenz(c,e)oxepine-5(7H)-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2=CC=CC=C2C3=CC=CC=C3C(=O)O1

Technology Process of dibenzo[c,e]oxepin-5(7H)-one

There total 36 articles about dibenzo[c,e]oxepin-5(7H)-one 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: 98.0%

: 3594-90-9
2,2'-bis(hydroxymethyl)biphenyl

: 4445-34-5
dibenz(C,E)oxepin-5(7H)-one

Guidance literature:: With [(η⁵-C₅Me₅)Ir(6,6'-dihydroxy-2,2'-bipyridine)(H₂O)]OTf₂; In water; for 6h; Inert atmosphere; Reflux; Green chemistry;
DOI:10.1002/cctc.201300717

Reference yield: 98.0%

: 13404-97-2
2'-(bromomethyl)<1,1'-biphenyl>-2-carboxaldehyde

: 4445-34-5
dibenz(C,E)oxepin-5(7H)-one

Guidance literature:: With oxygen; N-methyl-4,5-dimethylthiazolium iodide; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 50 ℃; for 0.25h; Reagent/catalyst; Temperature; Microwave irradiation;

Reference yield: 98.0%

: 64024-89-1
2'-Vinyl-2-biphenylmethanol

: 4445-34-5
dibenz(C,E)oxepin-5(7H)-one

Guidance literature:: With Oxone; osmium (III) chloride; In N,N-dimethyl-formamide; at 20 ℃; for 12h; Further Variations:; Catalysts; Product distribution;
DOI:10.1016/j.tetlet.2006.03.087