4-(2,4-Dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine

Base Information

• Chemical Name: 4-(2,4-Dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine
• CAS No.: 117844-98-1
• Molecular Formula: C₁₂H₁₄N₂O₂S
• Molecular Weight: 250.321
• Hs Code.: 2934100090
• DSSTox Substance ID: DTXSID80355388
• Wikidata: Q82134254
• ChEMBL ID: CHEMBL4210629
• Mol file: 117844-98-1.mol

Synonyms:117844-98-1;4-(2,4-dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine;4-(2,4-Dimethoxyphenyl)-5-methylthiazol-2-amine;Cambridge id 6872366;Oprea1_181688;CHEMBL4210629;DTXSID80355388;MFCD03145141;STL222604;AKOS000124015;BS-36808;CS-0335135;AB00121932-01;SR-01000245147;SR-01000245147-1

Chemical Property of 4-(2,4-Dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine

Chemical Property:

• Vapor Pressure: 3.26E-06mmHg at 25°C
• Refractive Index: 1.599
• Boiling Point: 387.6°C at 760 mmHg
• Flash Point: 188.2°C
• PSA: 85.61000
• Density: 1.227g/cm³
• LogP: 3.29910
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 250.07759887
• Heavy Atom Count: 17
• Complexity: 255

Purity/Quality:

99% ^*data from raw suppliers

4-(2,4-Dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(N=C(S1)N)C2=C(C=C(C=C2)OC)OC

Technology Process of 4-(2,4-Dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine

There total 2 articles about 4-(2,4-Dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine 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: 80.0%

2-Bromo-1-(2,4-dimethoxy-phenyl)-propan-1-one (117844-88-9) + thiourea (17356-08-0) → 4-(2,4-dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine (117844-98-1)

Guidance literature:

In ethanol; Heating;

Reference yield:

2,4-dimethoxypropiophenone (831-00-5) → 4-(2,4-dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine (117844-98-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / Br₂ / CCl₄ / 30 - 35 °C

2: 80 percent / ethanol / Heating

With bromine; In tetrachloromethane; ethanol;

Reference yield: 80.0%

acetic anhydride (108-24-7) + 4-(2,4-dimethoxyphenyl)-5-methyl-1,3-thiazol-2-amine (117844-98-1) → N-[4-(2,4-Dimethoxy-phenyl)-5-methyl-thiazol-2-yl]-acetamide (117845-00-8)

Guidance literature:

In benzene; Heating;

upstream raw materials:

2-Bromo-1-(2,4-dimethoxy-phenyl)-propan-1-one

thiourea

2,4-dimethoxypropiophenone

Downstream raw materials:

N-[4-(2,4-Dimethoxy-phenyl)-5-methyl-thiazol-2-yl]-acetamide

N-[4-(2,4-Dimethoxy-phenyl)-5-methyl-thiazol-2-yl]-benzamide

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