5-(Phenylmethylene)-3-propyl-2-thioxo-4-thiazolidinone

Base Information

Chemical Name:5-(Phenylmethylene)-3-propyl-2-thioxo-4-thiazolidinone
CAS No.:245095-98-1
Molecular Formula:C₁₃H₁₃NOS₂
Molecular Weight:263.384
Hs Code.:
DSSTox Substance ID:DTXSID901210877

Synonyms:SCHEMBL10487963;DTXSID901210877;5-(Phenylmethylene)-3-propyl-2-thioxo-4-thiazolidinone;245095-98-1

Suppliers and Price of 5-(Phenylmethylene)-3-propyl-2-thioxo-4-thiazolidinone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 5-(Phenylmethylene)-3-propyl-2-thioxo-4-thiazolidinone

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:263.04385639
Heavy Atom Count:17
Complexity:345

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCN1C(=O)C(=CC2=CC=CC=C2)SC1=S

Technology Process of 5-(Phenylmethylene)-3-propyl-2-thioxo-4-thiazolidinone

There total 1 articles about 5-(Phenylmethylene)-3-propyl-2-thioxo-4-thiazolidinone 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: 23.2%

: 39123-31-4
3-propyl-2-thioxo-1,3-thiazolidin-4-one

: 100-52-7
benzaldehyde

: 245095-98-1
3-propyl-5-benzylidenerhodanine

Guidance literature:: In acetic anhydride; for 3h; Heating;

Reference yield:

: 245095-98-1
3-propyl-5-benzylidenerhodanine

: 3-propyl-5-benzylidene-2-selenorhodanine

Guidance literature:: Multi-step reaction with 2 steps

1: 160 °C

2: 32 percent / H₂Se / ethanol / 20 °C

With hydrogen selenide; In ethanol; 1: Methylation / 2: Substitution;