cas 53641-60-4, 2-PHENYLGLYCINONITRILE HYDROCHLORIDE | Articles data ｜lookchem

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53641-60-4

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Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides yield 1-amino-1H-indenes in two distinct pathways; the success of these annulations relies on the high electrophilicity of α-cyano arylgold carbenes to activate an ionic pathway.
Singh, Rahulkumar Rajmani,Pawar, Samir Kundlik,Huang, Min-Jie,Liu, Rai-Shung
supporting information
p. 11434 - 11437
(2016/09/23)

Preparation of α-aminothioamides from aldehydes
The conversion of aldehydes into α-aminonitriles and thence into imidazolidin-4-thiones has been studied.Hydrolysis of the appropriate imidazolidin-4-thiones gave thioamides of nine naturally occuring α-amino acids.The possible pre-biotic significance of these compounds is discussed.
Paventi, Martino,Edward, John T.
p. 282 - 289
(2007/10/02)

Antihypertensive agents. Synthesis and biological properties of 2-amino-4-aryl-2-imidazolines.
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Matier et al.
p. 901,902, 908
(2007/10/05)

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Chemical Properties

Melting Point: 164-165 °C (dec.)(lit.)
Boiling Point: 235.8°Cat760mmHg
Flash Point:96.4°C
Density: g/cm³
Vapor Pressure: 0.0491mmHg at 25°C
BRN: 4155088
PSA: 49.81000
LogP: 2.71228

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