cas 105995-16-2, 2-Thienyl-carbamic Acid Ethyl Ester | Articles data ｜lookchem

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105995-16-2

Articles about 105995-16-2Total 3 be found

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New and simple synthesis of acid azides, ureas and carbamates from carboxylic acids: Application of peptide coupling agents EDC and HBTU
Conversion of carboxylic acids into acid azides using peptide coupling agents, EDC and HBTU is described. The procedure is efficient, practical and applicable to a diverse range of carboxylic acids including N-protected amino acids. Using the same reagents, one-pot synthesis of ureas, dipeptidyl urea esters and carbamates from acids has also been achieved. The Royal Society of Chemistry 2010.
Sureshbabu, Vommina V.,Lalithamba,Narendra,Hemantha
experimental part
p. 835 - 840
(2010/06/20)

Microwave-assisted intramolecular cyclization of electron-rich heterocycle derivatives by a palladium-catalyzed coupling reaction
Nitrogenated heteropolycyclic systems were obtained by intramolecular palladium-catalyzed coupling reactions promoted by microwave irradiation. Georg Thieme Verlag Stuttgart.
Beccalli, Egle M.,Broggini, Gianluigi,Martinelli, Michela,Sottocornola, Silvia
p. 136 - 140
(2008/09/20)

ARE THIOPHENES ATTACKED AT SULPHUR BY NITRENES?
Ethyl azidoformate is shown to attack a range of thiophenes at sulphur giving transient S,N-ylides which can be trapped with acenaphthylene as adducts; thiophene yields self-trapped products also.
Meth-Cohn, Otto,Vuuren, Gerda van
p. 1105 - 1108
(2007/10/02)

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Chemical Properties

Boiling Point: 212 °C at 760 mmHg
Flash Point:82 °C
Density: 1.269 g/cm³
Vapor Pressure: 0.177mmHg at 25°C
Refractive Index: 1.586
PSA: 66.57000
LogP: 2.38950

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