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N-nitrosopiperazines

The elementary analysis is in agreement with the theoretical values. The starting l-amino-4-cyclopentylpiperazine (b.p. 80°-82°C/0.1 mm Hg) is obtained by alkylating N-nitrosopiperazine with cyclopentyl bromide in ethanol in the presence of NaHC03 and reducing the so-obtained l-nitroso-4-cyclopentylpiperazine with LiAIH4 in ethyl ether. [Pg.2980]

There are several preparative routes to N-nitrosopiperazines, illustrated by the following examples ... [Pg.262]

SYNS N -METHYL-N-NITROSOPIPERAZINE 1-METHYL-4-NITROSOPIPERAZINE N-NITROSO-N -METHYLPIPERAZIN (GERMAN) O N-NITROSO-N -METHYLPIPERAZINE... [Pg.1029]

METHYL-4-NITROSOPIPERAZINE see NKW500 N -METHYL-N-NITROSOPIPERAZINE see NKW500 N-METHYL-N-NTTROSO-1 -PROPANAMINE see MNAOOO... [Pg.1778]

See other pages where N-nitrosopiperazines is mentioned: [Pg.101]    [Pg.2980]    [Pg.271]    [Pg.549]    [Pg.101]    [Pg.2980]    [Pg.271]    [Pg.549]    [Pg.177]   
See also in sourсe #XX -- [ Pg.227 , Pg.243 ]



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