2-Phenyl-5-benzothiazolepropionic acid

Base Information

Chemical Name:2-Phenyl-5-benzothiazolepropionic acid
CAS No.:52321-54-7
Molecular Formula:C₁₆H₁₃NO₂S
Molecular Weight:283.351
Hs Code.:2934999090
DSSTox Substance ID:DTXSID40200345
Nikkaji Number:J65.540F
Wikidata:Q83073434
Mol file:52321-54-7.mol

Synonyms:2-phenyl-5-benzothiazolepropanoic acid;2-phenyl-5-benzothiazolepropionic acid;K 309;K-309

Suppliers and Price of 2-Phenyl-5-benzothiazolepropionic acid

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 2 raw suppliers

Chemical Property of 2-Phenyl-5-benzothiazolepropionic acid

Chemical Property:

Vapor Pressure:1.66E-10mmHg at 25°C
Boiling Point:492.3°Cat760mmHg
Flash Point:251.5°C
PSA：78.43000
Density:1.314g/cm³
LogP:3.98050
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:283.06669983
Heavy Atom Count:20
Complexity:343

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC3=C(S2)C=CC(=C3)CCC(=O)O

Technology Process of 2-Phenyl-5-benzothiazolepropionic acid

There total 2 articles about 2-Phenyl-5-benzothiazolepropionic acid 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:

: 52321-52-5
5-(2-chloro-ethyl)-2-phenyl-benzothiazole

: 52321-54-7
3-(2-phenyl-benzothiazol-5-yl)-propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: dimethylsulfoxide

2: aq. HCl

With hydrogenchloride; In dimethyl sulfoxide;
DOI:10.1021/jm00251a004