N-Cyclohexyl-5-(3-formyl-4-nitrophenoxy)-N-methylpentanamide

Base Information

Chemical Name:N-Cyclohexyl-5-(3-formyl-4-nitrophenoxy)-N-methylpentanamide
CAS No.:105728-11-8
Molecular Formula:C19H26N2O5
Molecular Weight:362.426
Hs Code.:
DSSTox Substance ID:DTXSID40548517
Wikidata:Q82427246
Mol file:105728-11-8.mol

Synonyms:105728-11-8;N-Cyclohexyl-5-(3-formyl-4-nitrophenoxy)-N-methylpentanamide;SCHEMBL10376832;DTXSID40548517

Suppliers and Price of N-Cyclohexyl-5-(3-formyl-4-nitrophenoxy)-N-methylpentanamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-Cyclohexyl-5-(3-formyl-4-nitrophenoxy)-N-methylpentanamide

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:362.18417193
Heavy Atom Count:26
Complexity:473

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C1CCCCC1)C(=O)CCCCOC2=CC(=C(C=C2)[N+](=O)[O-])C=O

Technology Process of N-Cyclohexyl-5-(3-formyl-4-nitrophenoxy)-N-methylpentanamide

There total 5 articles about N-Cyclohexyl-5-(3-formyl-4-nitrophenoxy)-N-methylpentanamide 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:

: 5454-83-1
5-bromovaleric acid methyl ester

: 105728-11-8
5-(3-Formyl-4-nitro-phenoxy)-pentanoic acid cyclohexyl-methyl-amide

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / K₂CO₃ / dimethylformamide

2: 75 percent / aq. KOH

3: oxalyl chloride / benzene; dimethylformamide / 0.5 h

4: aq. Na₂CO₃ / tetrahydrofuran / 1 h / Ambient temperature

With potassium hydroxide; oxalyl dichloride; sodium carbonate; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a012

Reference yield:

: 42454-06-8
2-nitro-5-hydroxybenzaldehyde

: 105728-11-8
5-(3-Formyl-4-nitro-phenoxy)-pentanoic acid cyclohexyl-methyl-amide

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / K₂CO₃ / dimethylformamide

2: 75 percent / aq. KOH

3: oxalyl chloride / benzene; dimethylformamide / 0.5 h

4: aq. Na₂CO₃ / tetrahydrofuran / 1 h / Ambient temperature

With potassium hydroxide; oxalyl dichloride; sodium carbonate; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a012

Reference yield:

: 105728-03-8
5-(3-Formyl-4-nitro-phenoxy)-pentanoic acid methyl ester

: 105728-11-8
5-(3-Formyl-4-nitro-phenoxy)-pentanoic acid cyclohexyl-methyl-amide

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / aq. KOH

2: oxalyl chloride / benzene; dimethylformamide / 0.5 h

3: aq. Na₂CO₃ / tetrahydrofuran / 1 h / Ambient temperature

With potassium hydroxide; oxalyl dichloride; sodium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a012