5-chloro-2-nitro-N-(2-phenoxyethyl)benzamide

Base Information

Chemical Name:5-chloro-2-nitro-N-(2-phenoxyethyl)benzamide
CAS No.:83725-62-6
Molecular Formula:C₁₅H₁₃ClN₂O₄
Molecular Weight:320.732
Hs Code.:
DSSTox Substance ID:DTXSID301256871

Synonyms:5-chloro-2-nitro-N-(2-phenoxyethyl)benzamide;83725-62-6;Benzamide, 5-chloro-2-nitro-N-(2-phenoxyethyl)-;DTXSID301256871;AKOS024511951;VU0646017-1;SR-01000922985;SR-01000922985-1;F5526-0099

Suppliers and Price of 5-chloro-2-nitro-N-(2-phenoxyethyl)benzamide

Supply Marketing:

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

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Chemical Property of 5-chloro-2-nitro-N-(2-phenoxyethyl)benzamide

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:320.0563846
Heavy Atom Count:22
Complexity:382

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)OCCNC(=O)C2=C(C=CC(=C2)Cl)[N+](=O)[O-]

Technology Process of 5-chloro-2-nitro-N-(2-phenoxyethyl)benzamide

There total 3 articles about 5-chloro-2-nitro-N-(2-phenoxyethyl)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: 80.0%

: 41994-44-9
5-chloro-2-nitrobenzoyl chloride

: 1758-46-9
2-phenoxyethanamine

: 83725-62-6
N-(2-Phenoxyethyl)-5-chloro-2-nitrobenzamide

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; water; Ambient temperature;
DOI:10.1002/jhet.5570190317

Reference yield:

: 83725-61-5
2-(2-phenoxyethyl)-1H-isoindole-1,3(2H)-dione

: 83725-62-6
N-(2-Phenoxyethyl)-5-chloro-2-nitrobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 39.5 g / hydrazium hydrate / methanol / 2 h / Heating

2: 80 percent / NaOH / H₂O; dioxane / Ambient temperature

With sodium hydroxide; hydrazine hydrate; In 1,4-dioxane; methanol; water;
DOI:10.1002/jhet.5570190317

Reference yield:

: 589-10-6
phenoxyethyl bromide

: 83725-62-6
N-(2-Phenoxyethyl)-5-chloro-2-nitrobenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / dimethylformamide / 1 h / 85 °C

2: 39.5 g / hydrazium hydrate / methanol / 2 h / Heating

3: 80 percent / NaOH / H₂O; dioxane / Ambient temperature

With sodium hydroxide; hydrazine hydrate; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570190317