- CasNo 588-64-7
- Purity 99%
High Quality Chinese Factory supply 588-64-7 BENZALDEHYDE PHENYLHYDRAZONE
- Molecular Formula: C13H12N2
- Molecular Weight: 196.252
- Vapor Pressure: 0.000201mmHg at 25°C
- Melting Point: 156°C
- Refractive Index: 1.567
- Boiling Point: 327.5 °C at 760 mmHg
- PKA: 13.65±0.10(Predicted)
- Flash Point: 151.9 °C
- PSA: 24.39000
- Density: 1.01g/cm3
- LogP: 3.20560
BENZALDEHYDE PHENYLHYDRAZONE(Cas 588-64-7) Usage
|
General Description |
Benzaldehyde phenylhydrazone is a compound derived from the reaction between benzaldehyde and phenylhydrazine, with potential applications in nanomaterials and light-sensitive technologies. It has been studied for its structural properties, particularly in the context of oxidation reactions, where it forms derivatives such as "benzaldehyde phenylhydrazone oxide." NMR studies suggest the existence of multiple isomeric forms (dl and meso) that can interconvert, with an activation enthalpy of about 14 kcal/mol. BENZALDEHYDE PHENYLHYDRAZONE's reactivity and structural versatility make it relevant for synthetic and materials chemistry applications. |
InChI:InChI=1/C13H12N2/c1-3-7-12(8-4-1)11-14-15-13-9-5-2-6-10-13/h1-11,15H/b14-11+
588-64-7 Relevant articles
Dual-parameter correlations on rate of dehydration step of a condensation reaction in aqueous solutions of ethanol, propan-2-ol and 2-methylpropan-2-ol
Habibi Yangjeh,Gholami,Mostaghim
, p. 884 - 889 (2001)
The reaction kinetics of the dehydration...
Synthesis of 1,1′-([1,1′-Biphenyl]-4,4′-diyl)bis(3-aryl-5-phenylformazans) and 1,1′-([1,1′-Biphenyl]-4,4′-diyl)bis(3-aryl-5-phenyl-5,6-dihydro-1,2,4,5-tetrazin-1-ium) Perchlorates
Alalwan, D. H. K.,Jassim, T.,Kostryukov, S. G.,Kozlov, A. Sh.,Masterova, Yu. Yu.,Tezikova, V. S.
, p. 1600 - 1607 (2021/12/13)
Abstract: New bis-formazans and bis(5,6-...
Broad-Spectrum Antifungal Agents: Fluorinated Aryl- and Heteroaryl-Substituted Hydrazones
Thamban Chandrika, Nishad,Dennis, Emily K.,Brubaker, Katelyn R.,Kwiatkowski, Stefan,Watt, David S.,Garneau-Tsodikova, Sylvie
supporting information, p. 124 - 133 (2020/10/20)
Fluorinated aryl- and heteroaryl-substit...
Nitrogen-modified graphene as a metal-free carbocatalyst for the solvent-free oxidative homo- and heterocoupling of amines
Ganbari, Alireza,Tavakol, Hossein
, (2021/11/04)
In this study, graphene oxide (GO) has b...
METHODS OF FORMING IMINES, IMINE-RELATED AND IMINE-DERIVED COMPOUNDS USING GREEN SOLVENTS
-
Paragraph 0186-0189, (2021/10/22)
The present disclosure relates to using ...
588-64-7 Process route
-
-
4406-67-1
benzyl-phenyl-diazene
-
-
614-31-3
N-benzyl-N-phenylhydrazine
-
-
62-53-3
aniline
-
-
100-46-9
benzylamine
-
-
588-64-7
benzaldehyde phenylhydrazone
| Conditions | Yield |
|---|---|
|
|
-
-
586-96-9
Nitrosobenzene
-
-
100-46-9
benzylamine
-
-
588-64-7
benzaldehyde phenylhydrazone
-
-
588-64-7
(E)-1-benzylidene-2-phenylhydrazine
-
-
495-48-7,55599-32-1
azoxybenzene
| Conditions | Yield |
|---|---|
|
With
acetic acid;
In
dichloromethane;
for 8h;
Solvent;
Reflux;
|
38%
36% 17% |
|
With
acetic acid;
In
toluene;
for 8h;
Solvent;
Reflux;
|
30%
24% 20% |
588-64-7 Upstream products
-
186581-53-3
diazomethane
-
917-64-6
methyl magnesium iodide
-
60-29-7
diethyl ether
-
17384-37-1
acetic acid-(benzylidene-phenyl-hydrazide)
588-64-7 Downstream products
-
4430-12-0
(phenylazo)benzaldoxime
-
583-46-0
5-benzylidene-2-thiohydantoin
-
111709-02-5
ethyl 3-benzylidene-2-phenylcarbazate
-
17384-37-1
acetic acid-(benzylidene-phenyl-hydrazide)
WANT TO PURCHASE
Please contact us and we will reply to you as soon as possible.