4-nitrobenzaldehyde N-phenylthiosemicarbazone

Base Information

Chemical Name:4-nitrobenzaldehyde N-phenylthiosemicarbazone
CAS No.:55753-69-0
Molecular Formula:C14H12N4O2S
Molecular Weight:300.341
Hs Code.:
European Community (EC) Number:668-764-3
Wikidata:Q76306189

Synonyms:MFCD07189526;STL016112;AKOS002207715;AKOS002246030;NCGC00328527-01;NCGC00335877-01;4-nitrobenzaldehyde N-phenylthiosemicarbazone;4-Nitrobenzaldehyde-4-phenylthiosemicarbazone;AB01321463-02;AB01327778-02;(2E)-2-(4-nitrobenzylidene)-N-phenylhydrazinecarbothioamide

Suppliers and Price of 4-nitrobenzaldehyde N-phenylthiosemicarbazone

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 4-nitrobenzaldehyde N-phenylthiosemicarbazone

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:300.06809681
Heavy Atom Count:21
Complexity:383

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=S)NN=CC2=CC=C(C=C2)[N+](=O)[O-]
Isomeric SMILES:C1=CC=C(C=C1)NC(=S)N/N=C/C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 4-nitrobenzaldehyde N-phenylthiosemicarbazone

There total 2 articles about 4-nitrobenzaldehyde N-phenylthiosemicarbazone 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:

: 555-16-8
4-nitrobenzaldehdye

: 5351-69-9
4-Phenyl-3-thiosemicarbazide

: 55753-69-0
4’-nitrobenzaldehyde-4-phenylthiosemicarbazone

Guidance literature:: With hydrogenchloride; In ethanol; Heating;
DOI:10.1007/BF00809296

Reference yield:

: 103-72-0
phenyl isothiocyanate

: 55753-69-0
4’-nitrobenzaldehyde-4-phenylthiosemicarbazone

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / ethanol / 20 °C

2: acetic acid / 4 h / 79 °C

With hydrazine hydrate; acetic acid; In ethanol;
DOI:10.1080/17415993.2016.1163698