[2-{(E)-[4-(Diethylamino)phenyl]diazenyl}-4-(trifluoromethyl)-1,3-thiazol-5-yl]methanol

Base Information

• Chemical Name: [2-{(E)-[4-(Diethylamino)phenyl]diazenyl}-4-(trifluoromethyl)-1,3-thiazol-5-yl]methanol
• CAS No.: 137929-16-9
• Molecular Formula: C15H17F3N4OS
• Molecular Weight: 358.387
• DSSTox Substance ID: DTXSID30577311
• Mol file: 137929-16-9.mol

Synonyms:137929-16-9;DTXSID30577311;[2-{(E)-[4-(Diethylamino)phenyl]diazenyl}-4-(trifluoromethyl)-1,3-thiazol-5-yl]methanol

Chemical Property of [2-{(E)-[4-(Diethylamino)phenyl]diazenyl}-4-(trifluoromethyl)-1,3-thiazol-5-yl]methanol

Chemical Property:

• XLogP3: 4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 6
• Exact Mass: 358.10751684
• Heavy Atom Count: 24
• Complexity: 412

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(CC)C1=CC=C(C=C1)N=NC2=NC(=C(S2)CO)C(F)(F)F

Technology Process of [2-{(E)-[4-(Diethylamino)phenyl]diazenyl}-4-(trifluoromethyl)-1,3-thiazol-5-yl]methanol

There total 2 articles about [2-{(E)-[4-(Diethylamino)phenyl]diazenyl}-4-(trifluoromethyl)-1,3-thiazol-5-yl]methanol 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: 56.0%

Ethyl 2-(4-N,N-diethylamino)phenylazo-4-trifluoromethylthiazole-5-carboxylate (137929-15-8) → 2-(4-N,N-Diethylamino)phenylazo-5-hydroxymethyl-4-trifluoromethylthiazole (137929-16-9)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; at -10 ℃; for 15h;

Reference yield:

ethyl 2-amino-4-(trifluoromethyl)-5-thiazole-carboxylate (344-72-9) → 2-(4-N,N-Diethylamino)phenylazo-5-hydroxymethyl-4-trifluoromethylthiazole (137929-16-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 1) nitrosylsulfuric acid / 1) acetic acid, 30 min, 2) acetic acid, 15-20 deg C, 15 h

2: 56 percent / LiAlH₄ / diethyl ether / 15 h / -10 °C

With lithium aluminium tetrahydride; nitrosylsulfuric acid; In diethyl ether;

Reference yield: 84.0%

2-(4-N,N-Diethylamino)phenylazo-5-hydroxymethyl-4-trifluoromethylthiazole (137929-16-9) → 2-(4-N,N-Diethylamino)phenylazo-4-trifluoromethylthiazole-5-carbaldehyde (137953-59-4)

Guidance literature:

With manganese(IV) oxide; In diethyl ether; for 5h; Ambient temperature;

upstream raw materials:

Ethyl 2-(4-N,N-diethylamino)phenylazo-4-trifluoromethylthiazole-5-carboxylate

ethyl 2-amino-4-(trifluoromethyl)-5-thiazole-carboxylate

Downstream raw materials:

2-(4-N,N-Diethylamino)phenylazo-4-trifluoromethylthiazole-5-carbaldehyde

5-(2,2-Dicyanovinyl)-2-(4-N,N-diethylamino)phenylazo-4-trifluoromethylthiazole

2-{2-[1-[2-(4-Diethylamino-phenylazo)-4-trifluoromethyl-thiazol-5-yl]-meth-(Z)-ylidene]-3-oxo-indan-1-ylidene}-malononitrile

2-{2-[1-[2-(4-Diethylamino-phenylazo)-4-trifluoromethyl-thiazol-5-yl]-1-piperidin-1-yl-meth-(E)-ylidene]-3-oxo-indan-1-ylidene}-malononitrile