N-(Acetyloxy)-N-((4-phenoxyphenyl)methoxy)benzamide

Base Information

Chemical Name:N-(Acetyloxy)-N-((4-phenoxyphenyl)methoxy)benzamide
CAS No.:139259-92-0
Molecular Formula:C22H19 N O5
Molecular Weight:377.397
Hs Code.:
UNII:CV01GZK8GV
DSSTox Substance ID:DTXSID70160983
Nikkaji Number:J436.381G
Wikidata:Q27275821
Mol file:139259-92-0.mol

Synonyms:139259-92-0;N-(Acetyloxy)-N-((4-phenoxyphenyl)methoxy)benzamide;[benzoyl-[(4-phenoxyphenyl)methoxy]amino] acetate;CCRIS 8766;UNII-CV01GZK8GV;CV01GZK8GV;Benzamide, N-(acetyloxy)-N-((4-phenoxyphenyl)methoxy);N-Acetoxy-N-[(4-phenoxybenzyl)oxy]benzamide;N-ACETOXY-N-((4-PHENOXYBENZYL)OXY)BENZAMIDE;N-(ACETYLOXY)-N-[(4-PHENOXYPHENYL)METHOXY]BENZAMIDE;DTXSID70160983;LS-25244;N-Acetoxy-N-(4-phenoxybenzyloxy)benzamide;Q27275821;ACETIC ACID, BENZOYL((4-PHENOXYPHENYL)METHOXY)AZANYL ESTER

Suppliers and Price of N-(Acetyloxy)-N-((4-phenoxyphenyl)methoxy)benzamide

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 1 raw suppliers

Chemical Property of N-(Acetyloxy)-N-((4-phenoxyphenyl)methoxy)benzamide

Chemical Property:

Vapor Pressure:5.72E-10mmHg at 25°C
Boiling Point:495.8°Cat760mmHg
Flash Point:253.7°C
PSA：65.07000
Density:1.248g/cm³
LogP:4.53100
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:377.12632271
Heavy Atom Count:28
Complexity:491

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)ON(C(=O)C1=CC=CC=C1)OCC2=CC=C(C=C2)OC3=CC=CC=C3

Technology Process of N-(Acetyloxy)-N-((4-phenoxyphenyl)methoxy)benzamide

There total 6 articles about N-(Acetyloxy)-N-((4-phenoxyphenyl)methoxy)benzamide 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: 78.0%

: 127-09-3
sodium acetate

: 139259-88-4
p-phenoxybenzyl N-chlorobenzohydroxamate

: 139259-92-0
N-(acetyloxy)-N-(((4-(phenyloxy)phenyl)methyl)oxy)benzamide

Guidance literature:: In acetone; Ambient temperature;

Reference yield:

: 36881-42-2
1-(bromomethyl)-4-phenoxybenzene

: 139259-92-0
N-(acetyloxy)-N-(((4-(phenyloxy)phenyl)methyl)oxy)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 65 percent / sodium carbonate / methanol; H₂O

2: tert-butyl hypochlorite / CH₂Cl₂ / 5 h

3: 78 percent / acetone / Ambient temperature

With tert-butylhypochlorite; sodium carbonate; In methanol; dichloromethane; water; acetone;

Reference yield:

: 93-89-0,99341-95-4
benzoic acid ethyl ester

: 139259-92-0
N-(acetyloxy)-N-(((4-(phenyloxy)phenyl)methyl)oxy)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 55 percent / potassium hydroxide, hydroxylamine hydrochloride / methanol

2: 65 percent / sodium carbonate / methanol; H₂O

3: tert-butyl hypochlorite / CH₂Cl₂ / 5 h

4: 78 percent / acetone / Ambient temperature

With potassium hydroxide; tert-butylhypochlorite; hydroxylamine hydrochloride; sodium carbonate; In methanol; dichloromethane; water; acetone;