4(5H)-Thiazolone, 5-(phenylmethylene)-2-(2-propen-1-ylthio)-, (5Z)-

Base Information

Chemical Name:4(5H)-Thiazolone, 5-(phenylmethylene)-2-(2-propen-1-ylthio)-, (5Z)-
CAS No.:521973-00-2
Molecular Formula:C₁₃H₁₁NOS₂
Molecular Weight:261.368
Hs Code.:
DSSTox Substance ID:DTXSID101161789

Synonyms:DTXSID101161789;4(5H)-Thiazolone, 5-(phenylmethylene)-2-(2-propen-1-ylthio)-, (5Z)-;521973-00-2

Suppliers and Price of 4(5H)-Thiazolone, 5-(phenylmethylene)-2-(2-propen-1-ylthio)-, (5Z)-

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
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Total 0 raw suppliers

Chemical Property of 4(5H)-Thiazolone, 5-(phenylmethylene)-2-(2-propen-1-ylthio)-, (5Z)-

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:261.02820632
Heavy Atom Count:17
Complexity:368

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C=CCSC1=NC(=O)C(=CC2=CC=CC=C2)S1
Isomeric SMILES:C=CCSC1=NC(=O)/C(=C/C2=CC=CC=C2)/S1

Technology Process of 4(5H)-Thiazolone, 5-(phenylmethylene)-2-(2-propen-1-ylthio)-, (5Z)-

There total 2 articles about 4(5H)-Thiazolone, 5-(phenylmethylene)-2-(2-propen-1-ylthio)-, (5Z)- 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: 82.0%

: 3806-42-6,174813-24-2
(Z)-5-benzylidene-2-thioxothiazolidin-4-one

: 556-56-9
allyl iodid

: 521973-00-2
5-((Z)-benzylidene)-2-allylmercapto-4-thiazolidinone

Guidance literature:: With sodium hydroxide; at 20 ℃;
DOI:10.1002/jhet.5570390607

Reference yield:

: 100-52-7
benzaldehyde

: 521973-00-2
5-((Z)-benzylidene)-2-allylmercapto-4-thiazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / sodium acetate / acetic acid / 3 h

2: 82 percent / aq. NaOH / 20 °C

With sodium hydroxide; sodium acetate; In acetic acid;
DOI:10.1002/jhet.5570390607