(2-(Trifluoromethyl)thiazol-4-yl)methanol

Base Information

• Chemical Name: (2-(Trifluoromethyl)thiazol-4-yl)methanol
• CAS No.: 133046-47-6
• Molecular Formula: C5H4F3NOS
• Molecular Weight: 183.1516
• Hs Code.: 2934100090
• European Community (EC) Number: 819-489-4
• DSSTox Substance ID: DTXSID40602209
• Wikidata: Q82499177
• Mol file: 133046-47-6.mol

Synonyms:(2-(Trifluoromethyl)thiazol-4-yl)methanol;133046-47-6;[2-(Trifluoromethyl)-1,3-thiazol-4-yl]methanol;C5H4F3NOS;4-Thiazolemethanol, 2-(trifluoromethyl)-;4-(Hydroxymethyl)-2-(trifluoromethyl)-1,3-thiazole;[2-(trifluoromethyl)thiazol-4-yl]methanol;(2-(trifluoromethyl)-1,3-thiazol-4-yl)methanol;2-(Trifluoromethyl)-4-thiazolemethanol;SCHEMBL1999685;DTXSID40602209;MFCD12963701;2-(Trifluoromethyl)4-thiazolemethanol;AKOS016007112;AM91876;2-trifluoromethyl-4-hydroxymethylthiazole;AS-35822;2-trifluoromethyl-1,3-thiazole-4-methanol;DB-344528;CS-0214585;EN300-181587;A904363;W-205415

Chemical Property of (2-(Trifluoromethyl)thiazol-4-yl)methanol

Chemical Property:

• Vapor Pressure: 0.709mmHg at 25°C
• Boiling Point: 176.8°C at 760 mmHg
• Flash Point: 60.7°C
• PSA: 61.36000
• Density: 1.533g/cm³
• LogP: 1.65420
• Storage Temp.: 2-8°C
• XLogP3: 1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 182.99656941
• Heavy Atom Count: 11
• Complexity: 140

Purity/Quality:

97% ^*data from raw suppliers

(2-(Trifluoromethyl)thiazol-4-yl)methanol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(N=C(S1)C(F)(F)F)CO

Technology Process of (2-(Trifluoromethyl)thiazol-4-yl)methanol

There total 3 articles about (2-(Trifluoromethyl)thiazol-4-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: 78.0%

→ (2-(trifluoromethyl)-1,3-thiazol-4-yl)methanol (133046-47-6)

Guidance literature:

Reference yield: 43.0%

Ethyl 2-(trifluoromethyl)thiazole-4-carboxylate (133046-46-5) → 2-(trifluoromethyl)-1,3-thiazole-4-carbaldehyde (133046-48-7) + (2-(trifluoromethyl)-1,3-thiazol-4-yl)methanol (133046-47-6)

Guidance literature:

With diisobutylaluminium hydride; In dichloromethane; at -78 ℃; for 1h;

Reference yield:

Ethyl 2-(trifluoromethyl)thiazole-4-carboxylate (133046-46-5) → (2-(trifluoromethyl)-1,3-thiazol-4-yl)methanol (133046-47-6)

Guidance literature:

With diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane; at -78 ℃; for 2h;

upstream raw materials:

Ethyl 2-(trifluoromethyl)thiazole-4-carboxylate

Downstream raw materials:

4-(chloromethyl)-2-(trifluoromethyl)thiazole

4-(bromomethyl)-2-(trifluoromethyl)thiazole