Benzaldehyde 4-nitrophenylhydrazone

Base Information

Chemical Name:Benzaldehyde 4-nitrophenylhydrazone
CAS No.:33786-33-3
Molecular Formula:C₁₃H₁₁N₃O₂
Molecular Weight:241.249
Hs Code.:
European Community (EC) Number:636-553-5
NSC Number:85453
UNII:QHV9RGK338
ChEMBL ID:CHEMBL3210082

Synonyms:Benzaldehyde 4-nitrophenylhydrazone;3078-09-9;1-benzylidene-2-(4-nitrophenyl)hydrazine;Benzaldehyde p-nitrophenylhydrazone;Benzal-4-nitrophenylhydrazone;Benzaldehyde, (p-nitrophenyl)hydrazone;Benzaldehyde, (4-nitrophenyl)hydrazone;BENZALDEHYDE-4-NITROPHENYLHYDRAZONE;33786-33-3;Benzaldehyde, 2-(4-nitrophenyl)hydrazone;NSC85453;(E)-1-benzylidene-2-(4-nitrophenyl)hydrazine;N-[(E)-benzylideneamino]-4-nitroaniline;(1E)-1-benzylidene-2-(4-nitrophenyl)hydrazine;MLS000859345;SCHEMBL3361105;CHEMBL3210082;NOIFWEYOLLHIMW-GXDHUFHOSA-N;(4-Nitrophenyl)hydrazonebenzaldehyde;MFCD00024596;NSC-85453;STK864454;AKOS003408199;benzaldehyde N-(4-nitrophenyl)hydrazone;NCGC00246703-01;SMR000461222;N-benzylidene-N'-(4-nitrophenyl)hydrazine;B0009;BENZALDEHYDE (4-NITROPHENYL)HYDRAZONE;CS-0327726;(E)-1-benzylidene-2-(4-nitrophenyl)hydrazone;J-018139

Suppliers and Price of Benzaldehyde 4-nitrophenylhydrazone

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of Benzaldehyde 4-nitrophenylhydrazone

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:241.085126602
Heavy Atom Count:18
Complexity:287

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=NNC2=CC=C(C=C2)[N+](=O)[O-]
Isomeric SMILES:C1=CC=C(C=C1)/C=N/NC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of Benzaldehyde 4-nitrophenylhydrazone

There total 1 articles about Benzaldehyde 4-nitrophenylhydrazone 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: 97.0%

: 100-52-7
benzaldehyde

: 100-16-3
4-nitrophenylhydrazone

: 33786-33-3
anti-benzaldehyde (4'-nitrophenyl)hydrazone

Guidance literature:: With acetic acid; In ethanol; for 3h; Reflux;
DOI:10.1039/b800502h

Reference yield: 73.0%

: 33786-33-3
anti-benzaldehyde (4'-nitrophenyl)hydrazone

: 25939-13-3
N-(p-nitrophenyl)benzohydrazonoyl chloride

Guidance literature:: With N-chlorosuccinimide-dimethyl sulfide; In dichloromethane; at -40 ℃;
DOI:10.1016/0040-4020(95)00916-7

Reference yield: 45.0%

: 62-53-3
aniline

: 33786-33-3
anti-benzaldehyde (4'-nitrophenyl)hydrazone

: 112080-55-4
N-(p-Nitrophenyl)-C,N'-diphenylformazan

Guidance literature:: With hydrogenchloride; tetrabutylammomium bromide; sodium carbonate; sodium nitrite; 2.) aq. CH₂Cl₂, 5 deg C to 15 deg C, 1 h;
DOI:10.1055/s-1995-3958