4-(4-nitrophenyl)-2-thiazolyl thiol

Base Information

Chemical Name:4-(4-nitrophenyl)-2-thiazolyl thiol
CAS No.:2104-10-1
Molecular Formula:C₉H₆N₂O₂S₂
Molecular Weight:238.291
Hs Code.:

Synonyms:4-(4-nitrophenyl)-2-thiazolyl thiol

Suppliers and Price of 4-(4-nitrophenyl)-2-thiazolyl thiol

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 0 raw suppliers

Chemical Property of 4-(4-nitrophenyl)-2-thiazolyl thiol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-(4-nitrophenyl)-2-thiazolyl thiol

There total 2 articles about 4-(4-nitrophenyl)-2-thiazolyl thiol 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:

: 513-74-6
ammonium dithiocarbamate

: 99-81-0
4-Nitrophenacyl bromide

: 2104-10-1
4-(4-nitrophenyl)-2-thiazolyl thiol

Guidance literature:: In ethanol; water; at 0 ℃; Reflux;
DOI:10.1080/10426507.2019.1700260

Reference yield:

: 2104-10-1
4-(4-nitro-phenyl)-3H-thiazole-2-thione

Guidance literature:: 2-Haloketon, NH4-dithiocarbamat;

Reference yield: 93.0%

: 2,2'-dimethyl-[1,1'-biphenyl]iodonium trifluoromethanesulfonate salt

: 2104-10-1
4-(4-nitrophenyl)-2-thiazolyl thiol

: (R)-2-((2'-iodo-6,6'-dimethyl-[1,1'-biphenyl]-2-yl)thio)-4-(4-nitrophenyl)thiazole

Guidance literature:: With (4R,4'R)-2,2'-(cyclopentane-1,1-diyl)-bis(4-phenyl-4,5-dihydrooxazole); copper diacetate; sodium carbonate; In dichloromethane; at 0 ℃; for 12h; enantioselective reaction;
DOI:10.1021/acs.orglett.9b04555