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2.6- Diamino-3-chloro-5-cyanopyrazine

Iminoethers were also prepared from 2-amino-3-cyanopyrazine with ethanolic hydrogen chloride (792, 1218) [the product with guanidine and sodium methoxide in methanol formed 2-amino-3-(C-guanidino-C-iminomethyl)pyrazine (878, 1218)] from 2,6-diamino-3-chloro-5-cyanopyrazine with ethanolic hydrogen chloride at 0 (the product heated with ethanol gave 2,6-diamino-3-chloro-5-triethoxymethyl-pyrazine) (1432) from 2-amino-5-chloro-3-cyanopyrazine the product with... [Pg.291]

A -(2 -imidazolin-2 -yl)amidino]pyrazine (59) (877)) and from 2,6-diamino-3-chloro-5-cyanopyrazine [the product heated with dimethylamine in ethanol at 40° gave 2,6-diamino-3-chloro-5-(A(,A -dimethylamidino)pyrazine] (1361). 2-Chloro-... [Pg.291]

The dipole moment of 2-chloro-3-cyanopyrazine has been determined as 3.44D in dioxane (749). Polymers have been prepared from 2,3-diamino-5,6-dicyano-... [Pg.289]


See other pages where 2.6- Diamino-3-chloro-5-cyanopyrazine is mentioned: [Pg.122]    [Pg.287]    [Pg.97]    [Pg.122]    [Pg.129]    [Pg.287]    [Pg.288]   


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2-Chloro-3-cyanopyrazine

2-Cyanopyrazine

3.5- Diamino-2-cyanopyrazine

Cyanopyrazines

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