2-chloro-N-[5-(2-chlorobenzyl)-1,3-thiazol-2-yl]acetamide

Base Information

• Chemical Name: 2-chloro-N-[5-(2-chlorobenzyl)-1,3-thiazol-2-yl]acetamide
• CAS No.: 301306-15-0
• Molecular Formula: C12H10Cl2N2OS
• Molecular Weight: 301.19
• European Community (EC) Number: 652-852-3
• Mol file: 301306-15-0.mol

Synonyms:301306-15-0;2-chloro-N-[5-(2-chlorobenzyl)-1,3-thiazol-2-yl]acetamide;2-chloro-N-{5-[(2-chlorophenyl)methyl]-1,3-thiazol-2-yl}acetamide;2-Chloro-N-(5-(2-chlorobenzyl)thiazol-2-yl)acetamide;2-chloro-N-[5-[(2-chlorophenyl)methyl]-1,3-thiazol-2-yl]acetamide;2-CHLORO-N-(5-(2-CHLOROBENZYL)-1,3-THIAZOL-2-YL)ACETAMIDE;BMA30615;STK952041;AKOS000533306;UPCMLD0ENAT5292183:001;CS-0222502;EN300-11137;SR-01000316806;SR-01000316806-1;Z57033992

Chemical Property of 2-chloro-N-[5-(2-chlorobenzyl)-1,3-thiazol-2-yl]acetamide

Chemical Property:

• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 299.9890895
• Heavy Atom Count: 18
• Complexity: 293

Purity/Quality:

99% ^*data from raw suppliers

2-CHLORO-N-[5-(2-CHLOROBENZYL)-1,3-THIAZOL-2-YL]ACETAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)CC2=CN=C(S2)NC(=O)CCl)Cl

Technology Process of 2-chloro-N-[5-(2-chlorobenzyl)-1,3-thiazol-2-yl]acetamide

There total 3 articles about 2-chloro-N-[5-(2-chlorobenzyl)-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:

2-chloro-3-(2-chloro-phenyl)-propionaldehyde (207463-28-3) → C12H10Cl2N2OS (301306-15-0)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol / Reflux

2: triethylamine / 1,4-dioxane

With triethylamine; In 1,4-dioxane; ethanol;

DOI:10.7124/bc.000971

Reference yield:

2-chlorobenzenediazonium chloride (89-90-7) → C12H10Cl2N2OS (301306-15-0)

Guidance literature:

Multi-step reaction with 3 steps

1: copper dichloride

2: ethanol / Reflux

3: triethylamine / 1,4-dioxane

With triethylamine; copper dichloride; In 1,4-dioxane; ethanol; 1: |Meerwein Arylation;

DOI:10.7124/bc.000971

Reference yield:

chloroacetyl chloride (79-04-9) + 5-(2-chlorobenzyl)-2-thiazolamine (207463-32-9) → C12H10Cl2N2OS (301306-15-0)

Guidance literature:

With triethylamine; In 1,4-dioxane;

DOI:10.7124/bc.000971

upstream raw materials:

2-chloro-3-(2-chloro-phenyl)-propionaldehyde

chloroacetyl chloride

5-(2-chlorobenzyl)-2-thiazolamine

2-chlorobenzenediazonium chloride

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