4-Acetamido-2-methoxy-5-nitrobenzoic acid

Base Information

Chemical Name:4-Acetamido-2-methoxy-5-nitrobenzoic acid
CAS No.:59338-94-2
Molecular Formula:C10H10N2O6
Molecular Weight:254.199
Hs Code.:
DSSTox Substance ID:DTXSID701253629
Wikidata:Q107860804

Synonyms:4-Acetamido-2-methoxy-5-nitrobenzoic acid;59338-94-2;SCHEMBL9835504;GEHILIYJUKFLNC-UHFFFAOYSA-N;DTXSID701253629;4-Acetamido-2-methoxy-5-nitrobenzoicacid;2-methoxy-4-acetamido-5-nitrobenzoic acid;4-(Acetylamino)-2-methoxy-5-nitrobenzoic acid;EN300-207661

Suppliers and Price of 4-Acetamido-2-methoxy-5-nitrobenzoic acid

Supply Marketing:

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

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Chemical Property of 4-Acetamido-2-methoxy-5-nitrobenzoic acid

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:254.05388604
Heavy Atom Count:18
Complexity:353

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=C(C=C(C(=C1)OC)C(=O)O)[N+](=O)[O-]

Technology Process of 4-Acetamido-2-methoxy-5-nitrobenzoic acid

There total 7 articles about 4-Acetamido-2-methoxy-5-nitrobenzoic acid 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: 64.9%

: 55304-05-7
4-acetylamino-2-methoxy-benzoic acid

: 59338-94-2
2-methoxy 4-acetylamino 5-nitro benzoic acid

Guidance literature:

Reference yield:

: 50-86-2
4-acetamidosalicylic acid

: 59338-94-2
2-methoxy 4-acetylamino 5-nitro benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 80 °C

2: sulfuric acid; acetic acid; nitric acid / 1 h / Cooling with ice

With sulfuric acid; nitric acid; potassium carbonate; acetic acid; In N,N-dimethyl-formamide;

Reference yield:

: 65-49-6
4-Aminosalicylic acid

: 59338-94-2
2-methoxy 4-acetylamino 5-nitro benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: acetone / 6 h

2: potassium carbonate / N,N-dimethyl-formamide / 12 h / 80 °C

3: sulfuric acid; acetic acid; nitric acid / 1 h / Cooling with ice

With sulfuric acid; nitric acid; potassium carbonate; acetic acid; In N,N-dimethyl-formamide; acetone;