N-Benzoyl-O-benzylhydroxylamine

Base Information

Chemical Name:N-Benzoyl-O-benzylhydroxylamine
CAS No.:3532-25-0
Molecular Formula:C14H13NO2
Molecular Weight:227.263
Hs Code.:2924299090
NSC Number:75238
DSSTox Substance ID:DTXSID80956753
Nikkaji Number:J104.683G
Wikidata:Q82936866
ChEMBL ID:CHEMBL1355102
Mol file:3532-25-0.mol

Synonyms:N-(Benzyloxy)benzamide;N-Benzoyl-O-benzylhydroxylamine;Benzamide, N-(benzyloxy)-;Benzamide, N-(phenylmethoxy)-;3532-25-0;Benzoic acid, O-benzyloxime;SMR000841564;benzylbenzhydroxamate;N-benzyloxybenzamide;NSC75238;benzoic acid O-benzyloxime;N-(Benzyloxy)benzamide #;MLS001243521;MLS002666830;SCHEMBL5120704;CHEMBL1355102;DTXSID80956753;HMS2208G10;HMS3352A19;N-(Benzyloxy)benzenecarboximidic acid;NSC-75238;AKOS008402633

Suppliers and Price of N-Benzoyl-O-benzylhydroxylamine

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

Total 6 raw suppliers

Chemical Property of N-Benzoyl-O-benzylhydroxylamine

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：38.33000
Density:1.154g/cm³
LogP:2.93910
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:227.094628657
Heavy Atom Count:17
Complexity:230

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of N-Benzoyl-O-benzylhydroxylamine

There total 32 articles about N-Benzoyl-O-benzylhydroxylamine 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: 100.0%

: 2687-43-6
O-benzylhydoxylamine hydrochloride

: 98-88-4
benzoyl chloride

: 3532-25-0
N-benzyloxy benzamide

Guidance literature:: With potassium carbonate; In water; ethyl acetate; at 0 - 20 ℃;
DOI:10.1039/d1ob00055a

Reference yield: 98.0%

: 7007-15-0
3-benzoyl-1,3-oxazolidin-2-one

: 622-33-3
N-benzyloxyamine

: 497-25-6
dimethylenecyclourethane

: 3532-25-0
N-benzyloxy benzamide

Guidance literature:: With samarium(III) trifluoromethanesulfonate; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/ol0263301

Reference yield: 96.0%

: 622-33-3
N-benzyloxyamine

: 65-85-0,8013-63-6
benzoic acid

: 3532-25-0
N-benzyloxy benzamide

Guidance literature:: benzoic acid; With N-ethyl-N,N-diisopropylamine; chlorophosphoric acid diphenyl ester; In N,N-dimethyl-formamide; at 0 ℃; for 0.166667h;

N-benzyloxyamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.833333h; Further stages.;
DOI:10.1002/jhet.5570450406