5-Benzylidene-3-(p-chlorophenyl)rhodanine

Base Information

• Chemical Name: 5-Benzylidene-3-(p-chlorophenyl)rhodanine
• CAS No.: 13036-93-6
• Molecular Formula: C16H10 Cl N O S2
• Molecular Weight: 331.8397
• Wikidata: Q76119982

Synonyms:5-Benzylidene-3-(p-chlorophenyl)rhodanine;BRN 1135686;13036-93-6;Rhodanine, 5-benzylidene-3-(p-chlorophenyl)-;(5E)-5-benzylidene-3-(4-chlorophenyl)-2-sulfanylidene-1,3-thiazolidin-4-one;C16-H10-Cl-N-O-S2;AKOS001485584;LS-143532;5-benzylidene-3-(4-chlorophenyl)-2-thioxo-1,3-thiazolidin-4-one;(5E)-5-benzylidene-3-(4-chlorophenyl)-2-thioxo-1,3-thiazolidin-4-one

Chemical Property of 5-Benzylidene-3-(p-chlorophenyl)rhodanine

Chemical Property:

• Vapor Pressure: 1.51E-09mmHg at 25°C
• Boiling Point: 484.6°Cat760mmHg
• Flash Point: 246.9°C
• PSA: 77.70000
• Density: 1.48g/cm³
• LogP: 4.81080
• XLogP3: 5.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 330.9892340
• Heavy Atom Count: 21
• Complexity: 451

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C=C2C(=O)N(C(=S)S2)C3=CC=C(C=C3)Cl
• Isomeric SMILES: C1=CC=C(C=C1)/C=C/2\C(=O)N(C(=S)S2)C3=CC=C(C=C3)Cl

Technology Process of 5-Benzylidene-3-(p-chlorophenyl)rhodanine

There total 1 articles about 5-Benzylidene-3-(p-chlorophenyl)rhodanine 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: 76.0%

3-(4-chloro-phenyl)-2-thioxo-thiazolidin-4-one (13037-55-3) + benzaldehyde (100-52-7) → 3-(4-chlorophenyl)-5-benzylidene-2-thio-4-thiazolidinone (13036-93-6)

Guidance literature:

With sodium acetate; acetic acid; for 5h; Heating;

Reference yield: 87.0%

2-aminopyridine (504-29-0) + 3-(4-chlorophenyl)-5-benzylidene-2-thio-4-thiazolidinone (13036-93-6) → 3-(4-chlorophenyl)-5--2-thio-4-thiazolidinone

Guidance literature:

With sodium acetate; In methanol; for 4h; Heating;

Reference yield: 62.0%

3-(4-chlorophenyl)-5-benzylidene-2-thio-4-thiazolidinone (13036-93-6) + ethyl 2-cyanoacetate (105-56-6) → 3-(4-Chloro-phenyl)-5-oxo-7-phenyl-2-thioxo-2,3,4,5-tetrahydro-thiazolo[4,5-b]pyridine-6-carbonitrile (126751-02-8)

Guidance literature:

With ammonium acetate; In acetic acid; at 150 - 170 ℃; for 4h;

upstream raw materials:

3-(4-chloro-phenyl)-2-thioxo-thiazolidin-4-one

benzaldehyde

Downstream raw materials:

3-(4-Chloro-phenyl)-5-oxo-7-phenyl-2-thioxo-2,3,4,5-tetrahydro-thiazolo[4,5-b]pyridine-6-carbonitrile

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