2,3-diphenylpropiononitrile
- Name 2,3-diphenylpropiononitrile
- CAS 3333-14-0
- Purity 99%
Product Details
Factory Supply industrial standard 2,3-diphenylpropiononitrile 3333-14-0 In Stock
- Molecular Formula: C15H13 N
- Molecular Weight: 207.275
- Vapor Pressure: 0.000162mmHg at 25°C
- Melting Point: 58 °C
- Boiling Point: 330.8°Cat760mmHg
- Flash Point: 162.7°C
- PSA： 23.79000
- Density: 1.07g/cm3
- LogP: 3.53648
2,3-diphenylpropiononitrile(Cas 3333-14-0) Usage
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Synthesis Reference(s) |
Tetrahedron Letters, 7, p. 1509, 1966 DOI: 10.1016/0005-2760(66)90119-6 |
InChI:InChI=1/C15H13N/c16-12-15(14-9-5-2-6-10-14)11-13-7-3-1-4-8-13/h1-10,15H,11H2
3333-14-0 Relevant articles
PHOTOCHEMICAL REACTIONS OF ARENECARBONITRILES WITH ALIPHATIC AMINES. 1. EFFECT OF ARENE STRUCTURE ON AMINYL VS. alpha -AMINOALKYL RADICAL FORMATION.
Lewis,Zebrowski,Correa
, p. 187 - 193 (1984)
The photochemical reactions of several s...
Rearrangements in Aryl Substituted α,β-Unsaturated Nitriles. A Collisional Activation Study
Madhusudanan, K. P.,Murthy, V. S.,Fraisse, D.
, p. 812 - 816 (1989)
The rearrangement reactions following el...
Enantioselective Arylcyanation of Styrenes via Copper-Catalyzed Radical Relay?
Chen, Pinhong,Liu, Guosheng,Zhuang, Weiwen
, p. 50 - 54 (2021)
The first copper-catalyzed enantioselect...
Crystalline C - C and C=C Bond-Linked Chiral Covalent Organic Frameworks
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, p. 369 - 381 (2021)
While crystalline covalent organic frame...
Rapid and Simple Access to α-(Hetero)arylacetonitriles from Gem-Difluoroalkenes
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A scalable cyanation of gem-difluoroalke...
Nickel/Cobalt-Catalyzed Reductive Hydrocyanation of Alkynes with Formamide as the Cyano Source, Dehydrant, Reductant, and Solvent
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, p. 283 - 288 (2020/12/01)
A Ni/Co co-catalyzed reductive hydrocyan...
Base-controlled chemoselectivity: direct coupling of alcohols and acetonitriles to synthesise α-alkylated arylacetonitriles or acetamides
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, p. 15200 - 15204 (2021/09/06)
We achieved chemoselective synthesis of ...
α-Alkylation of arylacetonitriles with primary alcohols catalyzed by backbone modified N-heterocyclic carbene iridium(i) complexes
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A series of backbone-modified N-heterocy...
3333-14-0 Process route
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-
6114-57-4
(Z)-2,3-diphenylacrylonitrile
-
-
100-51-6,185532-71-2
benzyl alcohol
-
-
3333-14-0
2,3-diphenylpropionitrile
-
-
100-52-7
benzaldehyde
| Conditions | Yield |
|---|---|
|
ruthenium-grafted hydrotalcite;
In
toluene;
at 180 ℃;
for 20h;
|
98 % Chromat.
|
-
-
93-97-0
benzoic acid anhydride
-
-
2510-95-4
2,3-diphenylacrylonitrile
-
-
3333-14-0
2,3-diphenylpropionitrile
-
-
5415-80-5
2,3-diphenylpropan-1-amine
-
-
33233-34-0
2-benzyl-3-oxo-2,3-diphenylpropanenitrile
| Conditions | Yield |
|---|---|
|
With
HRu(1,3-bis(6'-methyl-2'-pyridylimino)isoindoline)(PPh3)2; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
toluene;
at 100 ℃;
for 15h;
under 5931.67 Torr;
Sealed tube;
|
92%
|
3333-14-0 Upstream products
-
6114-57-4
(Z)-2,3-diphenylacrylonitrile
-
140-29-4
phenylacetonitrile
-
2372-45-4
sodium butanolate
-
100-44-7
benzyl chloride
3333-14-0 Downstream products
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116569-77-8
2-benzyl-2-phenyl-4-piperidino-butyronitrile
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22985-47-3
4-benzyl-6-dimethylamino-5-methyl-4-phenyl-hexan-3-one
-
62567-78-6
2-(5-Chloro-2-nitro-phenyl)-2,3-diphenyl-propionitrile
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62567-77-5
2-(3-Chloro-4-nitro-phenyl)-2,3-diphenyl-propionitrile
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