Benzamide, N-((4-cyanobenzoyl)oxy)-N-(phenylmethoxy)-

Base Information

Chemical Name:Benzamide, N-((4-cyanobenzoyl)oxy)-N-(phenylmethoxy)-
CAS No.:220168-52-5
Molecular Formula:C22H16 N2 O4
Molecular Weight:372.38
Hs Code.:
UNII:T2S3326LYK
DSSTox Substance ID:DTXSID30176469
Nikkaji Number:J1.075.795I
Wikidata:Q83046797
Mol file:220168-52-5.mol

Synonyms:CCRIS 8778;220168-52-5;Benzamide, N-((4-cyanobenzoyl)oxy)-N-(phenylmethoxy)-;N-((4-Cyanobenzoyl)oxy)-N-(phenylmethoxy)benzamide;Benzamide, N-[(4-cyanobenzoyl)oxy]-N-(phenylmethoxy)-;N-[(4-CYANOBENZOYL)OXY]-N-(PHENYLMETHOXY)BENZAMIDE;T2S3326LYK;DTXSID30176469;LS-26242;Benzoyl(phenylmethoxy)azanyl 4-cyanobenzoate;N-(Benzyloxy)-N-[(4-cyanobenzoyl)oxy]benzamide;Benzoic acid, 4-cyano-, benzoyl(phenylmethoxy)azanyl ester

Suppliers and Price of Benzamide, N-((4-cyanobenzoyl)oxy)-N-(phenylmethoxy)-

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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Total 0 raw suppliers

Chemical Property of Benzamide, N-((4-cyanobenzoyl)oxy)-N-(phenylmethoxy)-

Chemical Property:

Vapor Pressure:8.71E-12mmHg at 25°C
Boiling Point:541.4°Cat760mmHg
Flash Point:281.2°C
Density:1.32g/cm³
XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:372.11100700
Heavy Atom Count:28
Complexity:564

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CON(C(=O)C2=CC=CC=C2)OC(=O)C3=CC=C(C=C3)C#N

Technology Process of Benzamide, N-((4-cyanobenzoyl)oxy)-N-(phenylmethoxy)-

There total 2 articles about Benzamide, N-((4-cyanobenzoyl)oxy)-N-(phenylmethoxy)- 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:

: 3532-25-0
N-benzyloxy benzamide

: 220168-52-5
N-(benzyloxy)-N-((4-cyanobenzoyl)oxy)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: tert-butyl hypochlorite / CH₂Cl₂ / 5 h

2: 34 percent Chromat_. / acetone / Ambient temperature

With tert-butylhypochlorite; In dichloromethane; acetone;
DOI:10.1021/jo980863z

Reference yield:

: 17264-66-3
sodium 4-cyanobenzoate

: 112403-68-6
benzyl N-chlorobenzohydroxamate

: 220168-52-5
N-(benzyloxy)-N-((4-cyanobenzoyl)oxy)benzamide

Guidance literature:: In acetone; Ambient temperature;
DOI:10.1021/jo980863z

Reference yield:

: 220168-52-5
N-(benzyloxy)-N-((4-cyanobenzoyl)oxy)benzamide

: 619-65-8,333406-09-0
4-cyanobenzoic Acid

: N-benzoyl-N-(benzyloxy)nitrenium ion

Guidance literature:: With sulfuric acid; In [D₃]acetonitrile; water-d2; at 34.85 ℃; Rate constant; Thermodynamic data; bimolecular rate constant and Arrhenius data (ln A, ΔS<*>, E_a); acid-independent rate constants at 298-338 K;
DOI:10.1021/jo980863z