2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol

Base Information

Chemical Name:2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol
CAS No.:10505-59-6
Molecular Formula:C11H12 N2 O S
Molecular Weight:220.2908
Hs Code.:
Mol file:10505-59-6.mol

Synonyms:4-Thiazoline-3-ethanol,2-imino-a-phenyl- (7CI,8CI); 2-Imino-3-(b-hydroxyphenethyl)thiazoline;2-Imino-a-phenyl-3(2H)-thiazoleethanol;NSC 315204

Suppliers and Price of 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol

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

Total 5 raw suppliers

Chemical Property of 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol

Chemical Property:

Vapor Pressure:1.45E-06mmHg at 25°C
Boiling Point:383.5°Cat760mmHg
Flash Point:185.7°C
Density:1.28g/cm³

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol

There total 3 articles about 2-[(2Z)-2-imino-1,3-thiazol-3(2H)-yl]-1-phenylethanol 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: 72.0%

: 116923-07-0
2-amino-3-(2-oxo-2-phenyl-ethyl)-thiazolium; bromide

: 10505-59-6
2-(2-imino-thiazol-3-yl)-1-phenyl-ethanol

Guidance literature:: With sodium tetrahydroborate; In methanol;

Reference yield:

: 70-11-1
α-bromoacetophenone

: 10505-59-6
2-(2-imino-thiazol-3-yl)-1-phenyl-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / acetonitrile / 12 h / 10 °C

2: 72 percent / sodium borohydride / methanol

With sodium tetrahydroborate; In methanol; acetonitrile;