2-Chloro-4-ethoxy-1-nitrobenzene

Base Information

Chemical Name:2-Chloro-4-ethoxy-1-nitrobenzene
CAS No.:5391-55-9
Molecular Formula:C₈H₈ClNO₃
Molecular Weight:201.609
Hs Code.:
DSSTox Substance ID:DTXSID401301859

Synonyms:2-chloro-4-ethoxy-1-nitrobenzene;5391-55-9;SCHEMBL10628038;DTXSID401301859;MFCD23719453;AKOS017443093;SY290329;CS-0453403;E86258

Suppliers and Price of 2-Chloro-4-ethoxy-1-nitrobenzene

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-Chloro-4-ethoxy-1-nitrobenzene

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:201.0192708
Heavy Atom Count:13
Complexity:183

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC1=CC(=C(C=C1)[N+](=O)[O-])Cl

Technology Process of 2-Chloro-4-ethoxy-1-nitrobenzene

There total 10 articles about 2-Chloro-4-ethoxy-1-nitrobenzene 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: 96.0%

: 64-17-5
ethanol

: 2106-50-5
2-chloro-4-fluoro-1-nitrobenzene

: 5391-55-9
3-chloro-4-nitro-phenetole

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 40 ℃; for 7h;

Reference yield:

: 116496-78-7
N-(5-ethoxy-2-nitrophenyl)acetamide

: 5391-55-9
3-chloro-4-nitro-phenetole

Guidance literature:: Multi-step reaction with 2 steps

1: NaOEt / ethanol

2: (i) (diazotization), (ii) CuCl

With sodium ethanolate; In ethanol;
DOI:10.1021/ja00865a031

Reference yield:

: 591-33-3
3-ethoxyacetanilide

: 5391-55-9
3-chloro-4-nitro-phenetole

Guidance literature:: Multi-step reaction with 3 steps

1: aq. HNO₃, Ac₂O

2: NaOEt / ethanol

3: (i) (diazotization), (ii) CuCl

With nitric acid; sodium ethanolate; acetic anhydride; In ethanol;
DOI:10.1021/ja00865a031