(2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide

Base Information

Chemical Name:(2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide
CAS No.:300829-00-9
Molecular Formula:C₁₂H₁₀N₂OS
Molecular Weight:230.29
Hs Code.:
DSSTox Substance ID:DTXSID90350223
Wikidata:Q82126051
ChEMBL ID:CHEMBL4208318
Mol file:300829-00-9.mol

Synonyms:(2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide;300829-00-9;(E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide;1415662-56-4;N-(thiazol-2-yl)cinnamamide;CHEMBL4208318;Cinnamamide, N-(2-thiazolyl)-;DTXSID90350223;HKTMXBUQDTYWOK-VOTSOKGWSA-N;HMS1428J15;STK005645;3-Phenyl-N-(thiazol-2-yl)acrylamide;AKOS000484895;IDI1_011248;(E)-3-Phenyl-N-(thiazol-2-yl)acrylamide;AB00075085-01;SR-01000396299;SR-01000396299-1;Z28173662;(2E)-3-Phenyl-N-(1,3-thiazol-2-yl)-2-propenamide #;F1443-4649;(E)-3-PHENYL-N~1~-(1,3-THIAZOL-2-YL)-2-PROPENAMIDE

Suppliers and Price of (2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide

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

Aronis compounds
3-phenyl-N-1,3-thiazol-2-ylacrylamide
20mg
$ 30.00

Total 1 raw suppliers

Chemical Property of (2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:230.05138412
Heavy Atom Count:16
Complexity:262

Purity/Quality:: 3-phenyl-N-1,3-thiazol-2-ylacrylamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=CC(=O)NC2=NC=CS2
Isomeric SMILES:C1=CC=C(C=C1)/C=C/C(=O)NC2=NC=CS2

Technology Process of (2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide

There total 5 articles about (2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide 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: 94.0%

: 96-50-4
2-thiazolylamine

: 140-10-3
(E)-3-phenylacrylic acid

: 300829-00-9
(2E)-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide

Guidance literature:: With N,N-dimethyl-formamide; dicyclohexyl-carbodiimide; In neat (no solvent); at 135 ℃; for 0.05h; Microwave irradiation;
DOI:10.1080/00397911.2011.604148