Ethyl 4-(3-nitrophenyl)thiazole-2-carboxylate

Base Information

• Chemical Name: Ethyl 4-(3-nitrophenyl)thiazole-2-carboxylate
• CAS No.: 53101-05-6
• Molecular Formula: C12H10N2O4S
• Molecular Weight: 278.288
• DSSTox Substance ID: DTXSID901205783
• Mol file: 53101-05-6.mol

Synonyms:Ethyl 4-(3-nitrophenyl)thiazole-2-carboxylate;53101-05-6;Ethyl 4-(3-nitrophenyl)-1,3-thiazole-2-carboxylate;2-Thiazolecarboxylic acid, 4-(3-nitrophenyl)-, ethyl ester;MFCD11976484;Ethyl4-(3-Nitrophenyl)thiazole-2-carboxylate;SCHEMBL7091428;ORZHIBZDQVVYKZ-UHFFFAOYSA-N;DTXSID901205783;AKOS010644302;AS-32065;SY024371;CS-0314724;A870821;4-(3-Nitrophenyl)thiazole-2-carboxylic acid ethyl ester;4-(3-nitrophenyl)-thiazole-2-carboxylic acid ethyl ester

Chemical Property of Ethyl 4-(3-nitrophenyl)thiazole-2-carboxylate

Chemical Property:

• PSA: 113.25000
• LogP: 3.41820
• XLogP3: 3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 278.03612798
• Heavy Atom Count: 19
• Complexity: 347

Purity/Quality:

97% ^*data from raw suppliers

Ethyl4-(3-nitrophenyl)thiazole-2-carboxylate 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)C1=NC(=CS1)C2=CC(=CC=C2)[N+](=O)[O-]

Technology Process of Ethyl 4-(3-nitrophenyl)thiazole-2-carboxylate

There total 3 articles about Ethyl 4-(3-nitrophenyl)thiazole-2-carboxylate 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: 83.0%

ethyl 2-amino-2-thioxoacetate (16982-21-1) + 3'-nitro-2-bromoacetophenone (2227-64-7) → 4-(3-nitro-phenyl)-thiazole-2-carboxylic acid ethyl ester (53101-05-6)

Guidance literature:

In ethanol; for 0.666667h; Heating;

DOI:10.1021/jm010496a

Reference yield:

3-Nitroacetophenone (121-89-1) → 4-(3-nitro-phenyl)-thiazole-2-carboxylic acid ethyl ester (53101-05-6)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridinium bromide perbromide, HBr / acetic acid / 0.5 h / Ambient temperature

2: ethanol / 30 h / Heating

With hydrogen bromide; pyridinium hydrobromide perbromide; In ethanol; acetic acid;

Reference yield:

→ 4-(3-nitro-phenyl)-thiazole-2-carboxylic acid ethyl ester (53101-05-6)

Guidance literature:

4-m-Nitro-ω-brom-acetophenon, Thiooxamethan;

upstream raw materials:

ethyl 2-amino-2-thioxoacetate

3'-nitro-2-bromoacetophenone

3-Nitroacetophenone

Downstream raw materials:

4-(3-amino-phenyl)-thiazole-2-carboxylic acid ethyl ester

4-(3-aminophenyl)thiazole-2-carboxylic acid amide

C₃₄H₃₉N₅O₅S

4-(3-(2-(5-cyclohexyl-1-(3,3-dimethyl-2-oxo-butyl)-2-oxo-1,2-dihydro-3H-1,3,4-benzotriazepin-3-yl)-acetylamino)-phenyl)-thiazole-2-carboxylic acid

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