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Top quality factory supply 868-54-2 2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE at low price
- Molecular Formula: C6H4N4
- Molecular Weight: 132.125
- Appearance/Colour: light pink to beige or light brownish
- Vapor Pressure: 1.84E-08mmHg at 25°C
- Melting Point: 171-173 °C (lit. )
- Refractive Index: 1.565
- Boiling Point: 591.9 °C at 760 mmHg
- PKA: -2.92±0.70(Predicted)
- Flash Point: 311.8 °C
- PSA： 97.39000
- Density: 1.262 g/cm3
- LogP: 0.86034
2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE(Cas 868-54-2) Usage
|
Biochem/physiol Actions |
2-Amino-1,1,3-propenetricarbonitrile is a key intermediate in synthesis of various heterocyclic compounds. 2-Amino-1,1-3-tricyanopropene undergoes condensation reaction with aromatic nitroso compounds to form useful coloring agents. 2-Amino-1,1-3-tricyanopropene reacts with 1,3-dithiole-derived polyenals to form push–pull systems with (Z)-geometry around the newly formed carbon-carbon double bond. |
InChI:InChI=1/C6H4N4/c7-2-1-6(10)5(3-8)4-9/h5,10H,1H2/b10-6+
868-54-2 Relevant articles
Copper-catalyzed tandem synthesis of pentasubstituted pyridines from sulfonoketenimides and 2-aminoprop-1-ene-1,1,3-tricarbonitrile
Yavari, Issa,Taheri, Zohreh,Nematpour, Manijeh,Sheikhi, Azam
, p. 2036 - 2038 (2014)
Fully substituted pyridines were synthes...
3-Trinitromethyl-4-nitro-5-nitramine-1: H-pyrazole: A high energy density oxidizer
Xiong, Hualin,Yang, Hongwei,Cheng, Guangbin
, p. 13827 - 13831 (2019)
A novel oxygen-rich energetic compound, ...
An Improved and Facile Synthesis of 2-Amino-1,1,3-tricyanopropene
Mittelbach, Martin
, p. 689 - 692 (1985)
A simple method for the dimerization of ...
Synthesis, antitumor evaluation, molecular modeling and quantitative structure-activity relationship (QSAR) of some novel arylazopyrazolodiazine and triazine analogs
El-Shafei, Ahmed,Fadda,Khalil,Ameen,Badria, Farid A.
, p. 5096 - 5105 (2009)
The synthesis, in vivo and in vitro anti...
Highly efficient diastereoselective synthesis of azabicyclo[22.2]octanes
Alizadeh, Abdolali,Sadeghi, Vahideh,Bayat, Fahimeh,Zhu, Long-Guan
, p. 2609 - 2612 (2014)
A one-pot, diastereoselective synthesis ...
Pyrazolo-oxo-diaza compound as BTK inhibitor
-
Paragraph 0113-0116, (2021/03/24)
The invention provides a pyrazolo-oxo-di...
Pyrazolo [1, 2] diaza compound
-
Paragraph 0032; 0113-0114, (2021/07/21)
The invention provides a pyrazolo [1, 2]...
Photocatalytic ?±-oxyamination of stable enolates, silyl enol ethers, and 2-oxoalkane phosphonic esters
Schroll, Peter,K??nig, Burkhard
supporting information, p. 309 - 313 (2015/03/03)
Fast ?±-oxyamination of stable enolates,...
868-54-2 Process route
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64-17-5
ethanol
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10544-72-6
dinitrogen tetraoxide
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109-77-3
malononitrile
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-
868-54-2
1,1,3-tricyano-2-amino-1-propene
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-
105-56-6
ethyl 2-cyanoacetate
Conditions
| Conditions | Yield |
|---|---|
|
Reaktion der Natrium-Verbindung;
|
-
-
109-77-3
malononitrile
-
-
868-54-2
1,1,3-tricyano-2-amino-1-propene
Conditions
| Conditions | Yield |
|---|---|
|
With
potassium hydroxide;
In
ethanol;
for 0.5h;
Product distribution;
Heating;
further solvents and reagents;
|
87%
|
|
With
potassium hydroxide;
In
ethanol;
for 0.5h;
Heating;
|
87%
|
|
With
sodium hydride;
In
dimethyl sulfoxide; paraffin oil;
at 20 ℃;
|
87%
|
|
With
sodium ethanolate;
In
ethanol;
Reflux;
|
82%
|
|
With
sodium hydroxide;
In
ethanol;
for 1h;
Reflux;
|
82%
|
|
With
tetrahydrofuran; diethyl ether; sodium;
|
|
|
With
sodium; benzene;
|
|
|
With
sodium ethanolate;
|
|
|
With
hydrogenchloride; benzene;
|
|
|
With
ammonium hydroxide;
|
|
|
With
sodium ethanolate;
|
|
|
With
potassium hydroxide;
In
various solvent(s);
|
|
|
With
sodium ethanolate;
|
|
|
With
sodium hydride;
In
dichloromethane;
at 20 ℃;
for 0.5h;
|
|
|
With
sodium hydroxide;
In
ethanol;
at 50 ℃;
for 0.5h;
Solvent;
Temperature;
|
|
|
With
sodium hydroxide;
In
ethanol;
|
868-54-2 Upstream products
-
109-99-9
tetrahydrofuran
-
60-29-7
diethyl ether
-
109-77-3
malononitrile
-
71-43-2
benzene
868-54-2 Downstream products
-
54711-21-6
5-amino-3-(cyanomethyl)-1H-pyrazole-4-carbonitrile
-
7152-40-1
5-amino-3-(cyanomethyl)-1-phenyl-1H-pyrazole-4-carbonitrile
-
100991-84-2
2-amino-4-(4-dimethylaminophenyl)buta-1,3-diene-1,1,3-tricarbonitrile
-
106276-41-9
2-amino-3-(4-dimethylamino-phenylimino)-propene-1,1,3-tricarbonitrile
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