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1229-55-6

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An environmentally friendly approach to the green synthesis of azo dyes with aryltriazenes via ionic liquid promoted C-N bonds formation
An efficient and green approach for the synthesis of azo dyes has been developed via the Br?nsted acidic ionic liquid (IL) promoted diazo coupling reaction of naphthols with aryltriazenes. The reaction was carried out with the aryltriazenes as diazotizing
Zhang, Yonghong,Liu, Yonghong,Ma, Xiaoqian,Ma, Xia,Wang, Bin,Li, Hongguang,Huang, Yan,Liu, Chenjiang
p. 438 - 444
(2018/06/14)

New dry arenediazonium salts, stabilized to an exceptionally high degree by the anion of o-benzenedisulfonimide
Arenediazonium o-benzenedisulfonimides 3 (20 examples, yield >90%) were prepared in the dry state by diazotization of aromatic amines with (-pentyl nitrite and o-benzenedisulfonimide in glacial acetic acid or formic acid at 0-5°C. Unlike most diazonium salts in the dry state, salts 3 are very highly stable.
Barbero, Margherita,Crisma, Marco,Degani, Lacopo,Fochi, Rita,Perracino, Paolo
p. 1171 - 1175
(2007/10/03)

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Chemical Properties

Appearance/Colour :Odorless, red powder.
Melting Point: 179 °C
Boiling Point: 490.978 °C at 760 mmHg
Flash Point:250.735 °C
Density: 1.194 g/cm³
Storage Temp.:room temp
Vapor Pressure: 0mmHg at 25°C
Refractive Index: 1.616
PKA: 13.61±0.50(Predicted)
BRN: 1843558
PSA: 54.18000
LogP: 4.96940

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