N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)methoxy)benzamide

Base Information

Chemical Name:N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)methoxy)benzamide
CAS No.:139259-93-1
Molecular Formula:C20H23 N O4
Molecular Weight:341.407
Hs Code.:
UNII:HM1A80K8JX
DSSTox Substance ID:DTXSID30160984
Nikkaji Number:J436.382E
Wikidata:Q27279997
Mol file:139259-93-1.mol

Synonyms:139259-93-1;CCRIS 8770;N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)methoxy)benzamide;UNII-HM1A80K8JX;HM1A80K8JX;N-Acetoxy-N-[(4-tert-butylbenzyl)oxy]benzamide;Benzamide, N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)methoxy)-;[benzoyl-[(4-tert-butylphenyl)methoxy]amino] acetate;N-Acetoxy-N-(4-tert-butylbenzyloxy)benzamide;N-(ACETYLOXY)-N-[[4-(1,1-DIMETHYLETHYL)PHENYL]METHOXY]BENZAMIDE;DTXSID30160984;LS-25234;Q27279997;N-ACETOXY-N-((4-(TERT-BUTYL)BENZYL)OXY)BENZAMIDE;ACETIC ACID, BENZOYL((4-(1,1-DIMETHYLETHYL)PHENYL)METHOXY)AZANYL ESTER

Suppliers and Price of N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)methoxy)benzamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)methoxy)benzamide

Chemical Property:

Vapor Pressure:8.1E-08mmHg at 25°C
Boiling Point:436.4°Cat760mmHg
Flash Point:217.7°C
PSA：55.84000
Density:1.143g/cm³
LogP:4.03620
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:341.16270821
Heavy Atom Count:25
Complexity:443

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)C(C)(C)C

Technology Process of N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)methoxy)benzamide

There total 6 articles about N-(Acetyloxy)-N-((4-(1,1-dimethylethyl)phenyl)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: 26.0%

: 127-09-3
sodium acetate

: 139259-86-2
p-tert-butylbenzyl N-chlorobenzohydroxamate

: 139259-93-1
N-(acetyloxy)-N-(((4-(1,1-dimethylethyl)phenyl)methyl)oxy)benzamide

Guidance literature:: In acetone; Ambient temperature;

Reference yield:

: 877-65-6
p-tert-butylbenzyl alcohol

: 139259-93-1
N-(acetyloxy)-N-(((4-(1,1-dimethylethyl)phenyl)methyl)oxy)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: HBr-H₂SO₄ / diethyl ether / Heating

2: 72 percent / sodium carbonate / methanol; H₂O

3: tert-butyl hypochlorite / CH₂Cl₂ / 5 h

4: 26 percent / acetone / Ambient temperature

With tert-butylhypochlorite; sulfuric acid; hydrogen bromide; sodium carbonate; In methanol; diethyl ether; dichloromethane; water; acetone;

Reference yield:

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

: 139259-93-1
N-(acetyloxy)-N-(((4-(1,1-dimethylethyl)phenyl)methyl)oxy)benzamide

Guidance literature:: Multi-step reaction with 4 steps

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

2: 72 percent / sodium carbonate / methanol; H₂O

3: tert-butyl hypochlorite / CH₂Cl₂ / 5 h

4: 26 percent / acetone / Ambient temperature

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