N,N-DIPHENYLACETAMIDE
Contact usGood factory supply good N,N-DIPHENYLACETAMIDE 519-87-9
- Molecular Formula: C14H13 N O
- Molecular Weight: 211.263
- Vapor Pressure: 5.26E-07mmHg at 25°C
-
Melting Point:
100-103 °C(lit.)
- Refractive Index: 1.5780 (estimate)
-
Boiling Point:
130 °C0.02 mm Hg(lit.)
- PKA: -3.21±0.50(Predicted)
- Flash Point: 199.7°C
- PSA: 20.31000
- Density: 1.125g/cm3
- LogP: 3.37120
N,N-DIPHENYLACETAMIDE(Cas 519-87-9) Usage
|
General Description |
N,N-Diphenylacetamide, also known as benzhydrol or DPA, is a chemical compound with the molecular formula C14H13NO. It is a white, crystalline solid that is soluble in organic solvents and insoluble in water. N,N-Diphenylacetamide is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It can also be used as a plasticizer, a fragrance ingredient, and a UV absorber in sunscreen formulations. The compound has been found to have antimicrobial and antioxidant properties and is currently under investigation for its potential use in various medical and industrial applications. However, it is important to handle N,N-Diphenylacetamide with caution as it may be harmful if ingested, inhaled, or in contact with the skin. |
InChI:InChI=1/C14H13NO/c1-12(16)15(13-8-4-2-5-9-13)14-10-6-3-7-11-14/h2-11H,1H3
519-87-9 Relevant articles
Hollow fiber liquid-phase microextraction with in situ derivatization combined with gas chromatography-mass spectrometry for the determination of root exudate phenylamine compounds in hot pepper (Capsicum annuum L.)
Sun, Haiyan,Wang, Yan
, p. 5494 - 5499 (2013)
Hollow fiber liquid-phase microextractio...
Preparation and catalytic evaluation of a palladium catalyst deposited over modified clinoptilolite (Pd&at;MCP) for chemoselective N-formylation and N-acylation of amines
Amirsoleimani, Mina,Khalilzadeh, Mohammad A.,Zareyee, Daryoush
, (2020/08/22)
Novel palladium nanoparticles stabilized...
Method for preparing aryl amide compound by catalyzing carbonylation of aryl tertiary amine through metal-free catalytic system
-
Paragraph 0028-0043; 0050-0063; 0066-0067, (2021/08/19)
The invention discloses a method for pre...
Nickel/Photoredox-Catalyzed Methylation of (Hetero)aryl Chlorides Using Trimethyl Orthoformate as a Methyl Radical Source
Kariofillis, Stavros K.,Shields, Benjamin J.,Tekle-Smith, Makeda A.,Zacuto, Michael J.,Doyle, Abigail G.
supporting information, p. 7683 - 7689 (2020/04/22)
Methylation of organohalides represents ...
Direct Synthesis of N,N-Disubstituted Formamides by Oxidation of Imines Using an HFIP/UHP System
Llopis, Natalia,Gisbert, Patricia,Baeza, Alejandro
, p. 11072 - 11079 (2020/10/12)
The straightforward synthesis of N,N-dis...
519-87-9 Process route
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103-84-4
Acetanilid
-
-
98-80-6
phenylboronic acid
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-
519-87-9
N,N-diphenylacetamide
| Conditions | Yield |
|---|---|
|
With
ammonium cerium (IV) nitrate; caesium carbonate;
In
acetonitrile;
at 20 ℃;
for 40h;
Reagent/catalyst;
Sealed tube;
Irradiation;
|
78%
|
|
With
copper diacetate; triethylamine;
In
dichloromethane;
for 48h;
Ambient temperature;
|
59%
|
|
With
pyridine; copper diacetate;
In
dichloromethane;
at 20 ℃;
for 48h;
|
35 %Chromat.
|
-
-
122-39-4
diphenylamine
-
-
75-36-5
acetyl chloride
-
-
519-87-9
N,N-diphenylacetamide
| Conditions | Yield |
|---|---|
|
With
iodine;
at 20 ℃;
for 0.0833333h;
Neat (no solvent);
|
97.58%
|
|
With
carbon-silica composite from starch (7.5 molpercent SO3H);
at 60 ℃;
for 0.45h;
solvent-free conditions;
|
96%
|
|
In
chloroform;
at 20 ℃;
for 4h;
|
78%
|
|
With
pyridine;
In
dichloromethane;
for 1h;
|
78%
|
|
With
silica gel;
at 20 ℃;
for 6.5h;
chemoselective reaction;
Green chemistry;
|
72%
|
|
In
chloroform;
at 0 - 5 ℃;
for 3h;
|
70.83%
|
|
With
ruthenium(III) 2,4-pentanedionate;
at 25 ℃;
for 24h;
|
65%
|
|
With
benzene;
|
|
|
With
pyridine; toluene;
|
|
|
With
pyridine; dibutyl ether;
|
|
|
|
|
|
With
triethylamine;
In
dichloromethane;
at 20 ℃;
for 12h;
|
|
|
With
triethylamine;
In
dichloromethane;
at 0 - 20 ℃;
for 24h;
|
519-87-9 Upstream products
-
506-96-7
Acetyl bromide
-
603-52-1
ethyl diphenylcarbamate
-
108-24-7
acetic anhydride
-
122-39-4
diphenylamine
519-87-9 Downstream products
-
61859-12-9
3t -[2]furyl-acrylic acid diphenylamide
-
611-64-3
9-methyl-acridine
-
2540-31-0
N,N-diphenylacetoacetamide
-
101-57-5
4-(phenylamino)benzenesulphonic acid
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