(2-(m-Tolyl)thiazol-4-yl)methanol

Base Information

Chemical Name:(2-(m-Tolyl)thiazol-4-yl)methanol
CAS No.:93476-40-5
Molecular Formula:C11H11NOS
Molecular Weight:205.28
Hs Code.:2934100090
DSSTox Substance ID:DTXSID90586186
Wikidata:Q82478263
Mol file:93476-40-5.mol

Synonyms:93476-40-5;(2-(m-Tolyl)thiazol-4-yl)methanol;(2-M-TOLYL-THIAZOL-4-YL)-METHANOL;[2-(3-METHYLPHENYL)-1,3-THIAZOL-4-YL]METHANOL;SCHEMBL12875865;DTXSID90586186;AKOS000320867;AB27077;DB-079595;CS-0362790;A1-33309

Suppliers and Price of (2-(m-Tolyl)thiazol-4-yl)methanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(2-m-Tolyl-thiazol-4-yl)-methanol
100mg
$ 200.00

Crysdot
(2-(m-Tolyl)thiazol-4-yl)methanol 97%
1g
$ 450.00

Anichem
(2-m-Tolyl-thiazol-4-yl)-methanol >95%
5g
$ 980.00

Anichem
(2-m-Tolyl-thiazol-4-yl)-methanol >95%
1g
$ 450.00

Alichem
(2-(m-Tolyl)thiazol-4-yl)methanol
1g
$ 441.00

A1 Biochem Labs
(2-(m-Tolyl)thiazol-4-yl)methanol 95%
2.5 g
$ 1050.00

Total 5 raw suppliers

Chemical Property of (2-(m-Tolyl)thiazol-4-yl)methanol

Chemical Property:

PSA：61.36000
LogP:2.61080
XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:205.05613515
Heavy Atom Count:14
Complexity:188

Purity/Quality:

98%min ^*data from raw suppliers

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC=C1)C2=NC(=CS2)CO

Technology Process of (2-(m-Tolyl)thiazol-4-yl)methanol

There total 3 articles about (2-(m-Tolyl)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:

: 92422-79-2
2-m-tolyl-thiazole-4-carbaldehyde

: 93476-40-5
(2-m-tolyl-thiazol-4-yl)-methanol

Guidance literature:: With potassium hydroxide;

Reference yield:

: 132089-33-9
ethyl 2-(m-tolyl)thiazole-4-carboxylate

: 93476-40-5
(2-m-tolyl-thiazol-4-yl)-methanol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1016/j.bioorg.2021.105015

Reference yield:

: 89152-40-9
4-(iodomethyl)-2-(m-tolyl)thiazole

: 93476-40-5
(2-m-tolyl-thiazol-4-yl)-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: hexamethylenetetramine / acetic acid

2: aq. KOH

With potassium hydroxide; hexamethylenetetramine; In acetic acid;