5-[(4-Chlorophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one

Base Information

• Chemical Name: 5-[(4-Chlorophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one
• CAS No.: 6318-37-2
• Molecular Formula: C10H6 Cl N O S2
• Molecular Weight: 255.749
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID701301727
• ChEMBL ID: CHEMBL1716804
• Mol file: 6318-37-2.mol

Synonyms:MLS002639377;CBMicro_032450;SCHEMBL1249069;CHEMBL1716804;DTXSID701301727;HMS3087M24;AKOS030653223;SMR001548822;UPCMLD0ENAT0508-8318:001;FT-0679498

Chemical Property of 5-[(4-Chlorophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one

Chemical Property:

• Vapor Pressure: 1.41E-06mmHg at 25°C
• Boiling Point: 399°C at 760 mmHg
• Flash Point: 195.1°C
• PSA: 86.49000
• Density: 1.54g/cm³
• LogP: 3.15760
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 254.9579339
• Heavy Atom Count: 15
• Complexity: 321

Purity/Quality:

5-(4-CHLOROBENZYLIDENE)RHODANINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1C=C2C(=O)NC(=S)S2)Cl

Technology Process of 5-[(4-Chlorophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one

There total 9 articles about 5-[(4-Chlorophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one 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: 96.2%

2-thioxo-4-thiazolidinone (141-84-4) + 4-chlorobenzaldehyde (104-88-1) → 5-(4-chlorobenzylidene)rhodanine (6318-37-2,81154-18-9)

Guidance literature:

With sodium acetate; acetic anhydride; In acetic acid; Heating;

Reference yield: 49.0%

2-thioxo-4-thiazolidinone (141-84-4) + benzylidene phenylamine (538-51-2) + N-(4-chlorobenzylidene)aniline (2362-79-0) → 5-benzylidene-2-thioxothiazolidin-4-one (3806-42-6,174813-24-2) + 5-(4-chlorobenzylidene)rhodanine (6318-37-2,81154-18-9)

Guidance literature:

at 110 ℃; for 0.166667h; Neat (no solvent);

DOI:10.1016/j.bmcl.2012.07.049

Reference yield:

3-Benzoyl-5-[1-(4-chloro-phenyl)-meth-(Z)-ylidene]-2-thioxo-thiazolidin-4-one → 5-(4-chlorobenzylidene)rhodanine (6318-37-2,81154-18-9) + benzoic acid (65-85-0,8013-63-6)

Guidance literature:

With hydrogen cation; In water;

DOI:10.1023/A:1015514217370

upstream raw materials:

5-chloromethylene-2-thioxo-thiazolidin-4-one

chlorobenzene

4-chlorobenzaldehyde

5-(1-methyl-3-oxo-butylidene)-2-thioxo-thiazolidin-4-one

Downstream raw materials:

3-(4-chlorophenyl)propionic amide

5-(4-chloro-benzylidene)-3-(tetra-O-acetyl-β-D-glucopyranosyl)-2-thioxo-thiazolidin-4-one

5-(p-Chlorobenzylidene)-3--4-oxo-thiazolidine-2-thione

5-(p-Chlorobenzylidene)-3--4-oxo-thiazolidine-2-thione