phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate

Base Information

Chemical Name:phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate
CAS No.:73918-29-3
Molecular Formula:C₁₉H₁₁F₃N₂O₄S₂
Molecular Weight:452.435
Hs Code.:

phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ<sup>2</sup>-thiazoline-4-carboxylate

Synonyms:phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate

Suppliers and Price of phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate

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 phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate

There total 2 articles about phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate 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:

: 73918-23-7
luciferin ethoxyvinyl ester

: 73918-29-3
phenyl 2-(6'-trifluoroacetoxy-2'-benzothiazolyl)-Δ²-thiazoline-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent Chromat_. / potassium phenoxide / dimethylsulfoxide; various solvent(s) / under high vacuum

2: 1 h / Ambient temperature

With potassium phenolate; In dimethyl sulfoxide;
DOI:10.1021/ja00529a051