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Quality products?make an important contribution to long-term revenue and profitability. Top quality factory supply 842-79-5 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole at low price
1.What is the 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole ?
Used in Pharmaceutical Applications:
2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole is used as a pharmaceutical agent for its antimicrobial, anticancer, and anti-inflammatory properties. Its diverse biological activities make it a promising candidate for the development of new drugs to treat various diseases and conditions.
Used in Agrochemical Applications:
In the agrochemical industry, 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole is used as a component in the development of pesticides and other agrochemical products. Its antimicrobial properties can contribute to the control of pests and diseases in agriculture, enhancing crop protection and yield.
Used in Material Science Applications:
2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole is used as a key component in the development of organic electronic materials. Its unique electronic and optical properties make it suitable for applications in organic light-emitting diodes (OLEDs), organic solar cells, and other electronic devices, contributing to advances in the field of material science and technology.
Overall, the diverse range of applications for 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole makes it a valuable compound in the field of chemical research and development, with potential to impact various industries.
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123-11-5
4-methoxy-benzaldehyde
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613-94-5
benzoic acid hydrazide
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![2-(4-methoxy-phenyl)-5-phenyl-[1,3,4]oxadiazole](/upload/2026/5/b06115e3f5b9487bb0cb81759e1d7bf0_927e89fc-2424-4722-99c1-c815a858297d.png)
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842-79-5
2-(4-methoxy-phenyl)-5-phenyl-[1,3,4]oxadiazole
| Conditions | Yield |
|---|---|
|
4-methoxy-benzaldehyde; benzoic acid hydrazide;
In
N,N-dimethyl-formamide;
at 60 ℃;
Inert atmosphere;
With
N-ethyl-N,N-diisopropylamine; eosin y;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 12h;
Irradiation;
Inert atmosphere;
|
96%
|
|
With
hydrogenchloride;
In
ethanol;
for 2h;
Reflux;
|
92%
|
|
With
trichloroisocyanuric acid;
In
ethanol;
at 20 ℃;
for 0.75h;
|
81%
|
|
With
1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate; silica gel;
for 0.416667h;
Microwave irradiation;
Green chemistry;
|
67%
|
|
With
1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate;
In
chloroform;
for 12h;
Reflux;
|
60%
|
|
ammonium cerium(IV) nitrate;
In
dichloromethane;
for 11h;
Heating;
|
45%
|
|
Multi-step reaction
with
2
steps
1: ethanol / Reflux
2: oxygen; copper(II) bis(trifluoromethanesulfonate); caesium carbonate / N,N-dimethyl-formamide / 18 h / 110 °C
With
oxygen; copper(II) bis(trifluoromethanesulfonate); caesium carbonate;
In
ethanol; N,N-dimethyl-formamide;
|
|
|
Multi-step reaction
with
2
steps
1: 6H(1+)
*Mo9
O40
PV3
(6-)
/ acetic acid / 1.33 h / Reflux
2: chromium(VI) oxide / acetic acid / Reflux
With
chromium(VI) oxide; 6H(1+)*Mo9O40PV3(6-);
In
acetic acid;
|
|
|
Multi-step reaction
with
2
steps
1: ethanol / Heating
2: sodium chlorate; platinum / methanol / 3 h / 20 °C / Electrochemical reaction
With
sodium chlorate; platinum;
In
methanol; ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: ethanol / 10 h / Reflux
2: tert-Butyl hypoiodite; carbonic acid dimethyl ester / 0.25 h / 20 °C
With
tert-Butyl hypoiodite; carbonic acid dimethyl ester;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: ethanol / 10 h / Reflux
2: potassium carbonate; tetra-(n-butyl)ammonium iodide; tert.-butylhydroperoxide / water; ethyl acetate / 1 h / 60 °C
With
tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide; potassium carbonate;
In
ethanol; water; ethyl acetate;
|
|
|
Multi-step reaction
with
2
steps
1: ethanol / Reflux
2: potassium carbonate; iodine / dimethyl sulfoxide / 100 °C
With
iodine; potassium carbonate;
In
ethanol; dimethyl sulfoxide;
|
|
|
Multi-step reaction
with
2
steps
1: hydrogenchloride / ethanol / 2 h / Reflux
2: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / Reflux
With
hydrogenchloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
ethanol; toluene;
|
|
|
Multi-step reaction
with
2
steps
1: methanol / Reflux
2: Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; magnesium sulfate; oxygen / dichloromethane / 6 h / 35 °C / Sealed tube; Green chemistry
With
Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen; magnesium sulfate;
In
methanol; dichloromethane;
|
|
|
Multi-step reaction
with
2
steps
1: dimethyl sulfoxide / 0.5 h / 60 °C
2: potassium iodide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dimethyl sulfoxide / 4.5 h / 0 - 25 °C
With
potassium iodide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
dimethyl sulfoxide;
|
|
|
Multi-step reaction
with
2
steps
1: ethanol / 20 °C
2: isobutyraldehyde; oxygen / acetone / 35 °C / 760.05 Torr
With
oxygen; isobutyraldehyde;
In
ethanol; acetone;
|
|
|
Multi-step reaction
with
2
steps
1: tert
-butyl alcohol / Reflux
2: sodium hypochlorite / tert
-butyl alcohol; water / 0 - 20 °C
With
sodium hypochlorite;
In
water; tert-butyl alcohol;
|
|
|
Multi-step reaction
with
2
steps
1: toluene / 2 h / Reflux
2: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / 4 h / Reflux
With
2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
toluene;
|
-
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3290-99-1
4-methoxybenzoic acid hydrazide
-
-
611-73-4
Benzoylformic acid
-
-
842-79-5
2-(4-methoxy-phenyl)-5-phenyl-[1,3,4]oxadiazole
| Conditions | Yield |
|---|---|
|
With
tetrabutylammonium acetate;
In
methanol;
at 20 ℃;
for 3h;
Electrochemical reaction;
Inert atmosphere;
|
87%
|
|
With
tert.-butylhydroperoxide; sodium carbonate; potassium iodide;
In
1,4-dioxane;
at 120 ℃;
for 5h;
Sealed tube;
|
83%
|
|
With
potassium carbonate;
In
N,N-dimethyl-formamide;
at 25 ℃;
for 24h;
Sealed tube;
Irradiation;
|
82%
|
|
With
Eosin Y;
In
N,N-dimethyl-formamide;
at 45 ℃;
for 12h;
Sealed tube;
Irradiation;
|
67%
|
2.What is the CAS number for 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole ?
The CAS number of 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole is 842-79-5.
More information of 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole 842-79-5 are:
|
CAS?Number |
842-79-5 |
|
Density |
1.182g/cm3 |
|
Boiling Point |
413.3°C at 760 mmHg |
|
Flash Point |
203.8°C |
|
Vapor Pressure |
1.16E-06mmHg at 25°C |
|
Refractive Index |
1.576 |
|
HS CODE |
2934999090 |
|
PSA |
48.15000 |
|
LogP |
3.41220 |
3.What are another words for 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole ?
Synonyms?for?2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole 842-79-5:1,3,4-Oxadiazole,2-(p-methoxyphenyl)-5-phenyl- (6CI,7CI,8CI);2-(4-Methoxyphenyl)-5-phenyl-1,3,4-oxadiazole; 2-(p-Anisyl)-5-phenyl-1,3,4-oxadiazole;2-(p-Methoxyphenyl)-5-phenyl-1,3,4-oxadiazole;2-Phenyl-5-(4-methoxyphenyl)-1,3,4-oxadiazole;2-Phenyl-5-(p-methoxyphenyl)-1,3,4-oxadiazole; NSC 90371
4.What is the molecular formula of 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole?
The chemical formula of ?2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole is?C15H12 N2 O2 which containing 15 Carbon atoms,12 Hydrogen atoms,2 Nitrogen atoms and 2 Oxygen atoms,and the molecular weight of??2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole?is 252.272.
5.What is 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole (842-79-5) used for?
2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole is a heterocyclic chemical compound that belongs to the oxadiazole family. It features a five-membered ring structure with one oxygen and two nitrogen atoms, along with a 4-methoxyphenyl and a phenyl group attached to it. 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole has demonstrated potential applications across various fields, such as pharmaceuticals, agrochemicals, and material science, due to its unique electronic and optical properties as well as its promising biological activities.
InChI:InChI=1/C15H12N2O2/c1-18-13-9-7-12(8-10-13)15-17-16-14(19-15)11-5-3-2-4-6-11/h2-10H,1H3
Relevant articles related to 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole:
|
Article |
Source |
|
Sodium hypochlorite-mediated synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from hydrazides and aldehydes |
Paidi, Karuna Raman,Kolli, Murali Krishna,Reddy, Eeda Koti,Pedakotla, Venkata Ramana , p. 371 - 376 (2020/05/04) |
|
Electrochemical Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazoles from α-Keto Acids and Acylhydrazines Under Mild Conditions |
Lu, Fangling,Gong, Fengping,Li, Liangsen,Zhang, Kan,Li, Zhen,Zhang, Xinwei,Yin, Ying,Wang, Ying,Gao, Ziwei,Zhang, Heng,Lei, Aiwen supporting information, p. 3257 - 3260 (2020/05/25) |
6.Buy 2-(4-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole with the best price .
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