2,6-Dichlorobenzaldehyde thiosemicarbazone

Base Information

• Chemical Name: 2,6-Dichlorobenzaldehyde thiosemicarbazone
• CAS No.: 24047-22-1
• Molecular Formula: C8H7Cl2N3S
• Molecular Weight: 248.136
• European Community (EC) Number: 653-627-2
• Wikidata: Q76305175
• Mol file: 24047-22-1.mol

Synonyms:2,6-Dichlorobenzaldehyde thiosemicarbazone;[(E)-(2,6-dichlorophenyl)methylideneamino]thiourea;24047-22-1;[(2,6-dichlorophenyl)methylideneamino]thiourea;(2E)-2-(2,6-dichlorobenzylidene)hydrazinecarbothioamide;SCHEMBL21519432;SCHEMBL21519523;JWTQZQFPOKSWPZ-UUILKARUSA-N;MFCD02656340;STK180702;STL302865;AKOS002240604;AKOS003408003;CCG-244058;NCGC00338330-01;2,6-Dichlorobenzaldehyde thiosemicarbazone #;CS-0336269;AB01330722-02;[(E)-(2,6-dichlorophenyl)methyleneamino]thiourea;AS-871/40441027;2-(2,6-dichlorobenzylidene)hydrazine-1-carbothioamide;F3284-2308;(2E)-2-(2,6-dichlorobenzylidene)hydrazinecarbimidothioic acid;(E)-2-(2,6-dichlorobenzylidene)hydrazinecarbimidothioic acid;Carbothioamide, 1-hydrazine-2-[1-(2,6-dichlorophenyl) methylidene];Hydrazinecarbothioamide, 2-[(2,6-dichlorophenyl)methylene]-, (2E)-

Chemical Property of 2,6-Dichlorobenzaldehyde thiosemicarbazone

Chemical Property:

• XLogP3: 2.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 246.9737738
• Heavy Atom Count: 14
• Complexity: 225

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC(=C(C(=C1)Cl)C=NNC(=S)N)Cl
• Isomeric SMILES: C1=CC(=C(C(=C1)Cl)/C=N/NC(=S)N)Cl

Technology Process of 2,6-Dichlorobenzaldehyde thiosemicarbazone

There total 2 articles about 2,6-Dichlorobenzaldehyde thiosemicarbazone 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: 85.0%

2,6-dichlorobenzaldehyde (83-38-5) + thiosemicarbazide (79-19-6) → 2-(2,6-dichlorobenzylidene)hydrazinecarbothioamide (24047-22-1)

Guidance literature:

In ethanol; water; for 1h; Heating;

Reference yield:

→ 2-(2,6-dichlorobenzylidene)hydrazinecarbothioamide (24047-22-1)

Guidance literature:

2,6-Dichlorbenzaldehyd, Thiosemicarbazid/EtOH;

Reference yield: 92.0%

2-(2,6-dichlorobenzylidene)hydrazinecarbothioamide (24047-22-1) + 2-(4-bromo-3-oxobutyl)phthalimide → 2-(2-(2-(2-(2,6-dichlorobenzylidene)hydrazinyl)thiazol-4-yl)ethyl)isoindoline-1,3-dione

Guidance literature:

In ethanol; for 20h; Reflux;

DOI:10.1016/j.bioorg.2021.104819

upstream raw materials:

2,6-dichlorobenzaldehyde

thiosemicarbazide

Downstream raw materials:

5-(2,6-dichlorophenyl)-1,3,4-thiadiazol-2-amine

[2-(2,6-Dichloro-phenyl)-4-oxo-thiazolidin-3-yl]-thiourea

2-{[1-(2,6-Dichloro-phenyl)-meth-(E)-ylidene]-hydrazono}-thiazolidin-4-one

2-Chloro-5-(2,6-dichloro-phenyl)-[1,3,4]thiadiazole

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