(benzylphenylamino)acetonitrile
- Name: (benzylphenylamino)acetonitrile
- CAS: 36271-19-9
- Purity: 99%
Details
Chinese Factory Supply Wholesale (benzylphenylamino)acetonitrile 36271-19-9 with Cheap Price
- Molecular Formula: C15H14N2
- Molecular Weight: 222.29
- Vapor Pressure: 2.34E-06mmHg at 25°C
- Melting Point: 193-194 °C
- Refractive Index: 1.62
- Boiling Point: 392.1 °C at 760 mmHg
- PKA: 0.96±0.50(Predicted)
- Flash Point: 172.9 °C
- PSA： 27.03000
- Density: 1.122 g/cm3
- LogP: 3.21678
(benzylphenylamino)acetonitrile(Cas 36271-19-9) Usage
|
General Description |
(Benzylphenylamino)acetonitrile is a chemical compound with the molecular formula C15H13N. It is a white to light beige crystalline powder that is insoluble in water but soluble in organic solvents. The compound is used as a building block in the synthesis of various pharmaceuticals and agrochemicals, particularly in the development of new drugs and active pharmaceutical ingredients. It is also employed as an intermediate in the production of dyes and pigments. Additionally, (Benzylphenylamino)acetonitrile has applications in research and development, particularly in the field of organic chemistry and chemical synthesis, where it serves as a versatile building block for the creation of new compounds and materials. Overall, (Benzylphenylamino)acetonitrile is a versatile chemical with various industrial and research applications. |
InChI:InChI=1/C15H14N2/c16-11-12-17(15-9-5-2-6-10-15)13-14-7-3-1-4-8-14/h1-10H,12-13H2
36271-19-9 Relevant articles
A new and convenient synthesis of antazoline derivatives
Dash,Kudav,Parihar
, p. 401 - 404 (2006)
Different N-benzyl anilines were N-alkyl...
Iron-catalyzed reductive strecker reaction
Yan, Fachao,Huang, Zijun,Du, Chen-Xia,Bai, Jian-Fei,Li, Yuehui
, p. 188 - 194 (2021/02/03)
Strecker reaction is widely applied for ...
Iron-catalysed carbene-transfer reactions of diazo acetonitrile
Empel, Claire,Hock, Katharina J.,Koenigs, Rene M.
supporting information, p. 7129 - 7133 (2018/10/24)
A continuous-flow protocol for the synth...
Iron-catalysed sequential reaction towards α-aminonitriles from secondary amines, primary alcohols and trimethylsilyl cyanide
Shen, Hang,Hu, Liangzhen,Liu, Qing,Hussain, Muhammad Ijaz,Pan, Jing,Huang, Mingming,Xiong, Yan
supporting information, p. 2776 - 2779 (2016/02/19)
We have developed a one-pot iron-catalys...
Alpha-aminonitrile synthetic method
-
Paragraph 0055; 0062; 0064, (2017/01/19)
The invention discloses a one-pot alpha-...
36271-19-9 Process route
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-
614-30-2
N-methyl-N-phenyl-benzenemethanamine
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![2-[benzyl(phenyl)amino]acetonitrile](/upload/2026/3/f5092c00961a47288f0e0eb5abdda0aa_14369a66-7528-4650-af5e-af75f012aa6b.png)
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36271-19-9
2-[benzyl(phenyl)amino]acetonitrile
| Conditions | Yield |
|---|---|
|
With
rhodium(III) chloride hydrate; dihydrogen peroxide;
In
water;
at 50 ℃;
for 4h;
|
92%
|
-
-
67-56-1
methanol
-
-
7677-24-9
trimethylsilyl cyanide
-
-
758640-21-0,103-32-2
N-Benzylaniline
-
-
36271-19-9
2-[benzyl(phenyl)amino]acetonitrile
| Conditions | Yield |
|---|---|
|
methanol; trimethylsilyl cyanide; N-Benzylaniline;
With
iron(II) oxalate;
In
toluene;
at 20 ℃;
Sealed tube;
With
tert.-butylhydroperoxide;
In
toluene; tert-butyl alcohol;
at 20 ℃;
for 4h;
Sealed tube;
|
26%
|
|
With
tert.-butylhydroperoxide; iron(II) oxalate;
In
toluene; tert-butyl alcohol;
at 90 ℃;
|
26%
|
36271-19-9 Upstream products
-
50-00-0
formaldehyd
-
758640-21-0
N-Benzylaniline
-
143-33-9
sodium cyanide
-
624-75-9
iodoacetonitrile
36271-19-9 Downstream products
-
408539-27-5
N -benzyl-N -phenyl-glycine amide
-
409111-05-3
N -benzyl-N -phenyl-thioglycine amide
-
91-75-8
antazoline
-
103401-89-4
1,2-bis-[2-(N -benzyl-anilinomethyl)-4,5-dihydro-imidazol-1-yl]-ethane
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