2-(4-formylphenoxy)-N-(1,3-thiazol-2-yl)acetamide

Base Information

• Chemical Name: 2-(4-formylphenoxy)-N-(1,3-thiazol-2-yl)acetamide
• CAS No.: 215503-93-8
• Molecular Formula: C12H10N2O3S
• Molecular Weight: 262.289
• DSSTox Substance ID: DTXSID90586222
• Wikidata: Q82478307
• Mol file: 215503-93-8.mol

Synonyms:215503-93-8;2-(4-FORMYLPHENOXY)-N-1,3-THIAZOL-2-YLACETAMIDE;2-(4-formylphenoxy)-N-(1,3-thiazol-2-yl)acetamide;2-(4-Formylphenoxy)-N-(thiazol-2-yl)acetamide;CHEMBRDG-BB 7865702;SCHEMBL15330952;DTXSID90586222;STL381210;AKOS000104705;MCULE-9157796232;DB-163211;2-(4-Formylphenoxy)-N-2-thiazolylacetamide;CS-0336430

Chemical Property of 2-(4-formylphenoxy)-N-(1,3-thiazol-2-yl)acetamide

Chemical Property:

• Density: 1.416g/cm³
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 262.04121336
• Heavy Atom Count: 18
• Complexity: 293

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1C=O)OCC(=O)NC2=NC=CS2

Technology Process of 2-(4-formylphenoxy)-N-(1,3-thiazol-2-yl)acetamide

There total 2 articles about 2-(4-formylphenoxy)-N-(1,3-thiazol-2-yl)acetamide 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: 66.0%

2-chloro-N-(1,3-thiazol-2-yl)acetamide (5448-49-7) + 4-hydroxy-benzaldehyde (123-08-0,65581-83-1) → 2-(4-formylphenoxy)-N-1,3-thiazol-2-ylacetamide (215503-93-8)

Guidance literature:

With sodium carbonate; In dimethyl sulfoxide; at 20 ℃; for 6h;

DOI:10.1134/S1070363220100254

Reference yield:

→ 2-(4-formylphenoxy)-N-1,3-thiazol-2-ylacetamide (215503-93-8)

Guidance literature:

With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane; for 3h; Reflux;

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 5 ℃; for 48h;

Reference yield: 62.0%

Cyanoacetohydrazide (140-87-4) + 2-(4-formylphenoxy)-N-1,3-thiazol-2-ylacetamide (215503-93-8) → 2-(4-{[2-(2-cyanoacetyl)hydrazono]-methyl}phenoxy)-N-(thiazol-2-yl)acetamide

Guidance literature:

In 1,4-dioxane; for 4h; Reflux;

DOI:10.1134/S1070363220100254

upstream raw materials:

2-chloro-N-(1,3-thiazol-2-yl)acetamide

4-hydroxy-benzaldehyde