1780-36-5Relevant articles and documents
Polyazidopyrimidines: High-energy compounds and precursors to carbon nanotubes
Ye, Chengfeng,Gao, Haixiang,Boatz, Jerry A.,Drake, Gregory W.,Twamley, Brendan,Shreeve, Jean'ne M.
, p. 7262 - 7265 (2006)
(Figure Presented) An additional azidomethyl group dramatically decreases the melting points of the corresponding azidopyrimidines. Theoretical calculations show that these polyazido compounds (see picture; N light blue, C dark blue, H white) exhibit high
Method for synthesizing 2,4,6,-trichlorine-5-methyl pyridine
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Paragraph 0018; 0021-0028, (2019/11/12)
The invention discloses a method for synthesizing 2,4,6,-trichlorine-5-methyl pyridine. The method for synthesizing the 2,4,6,-trichlorine-5-methyl pyridine comprises the steps that after the 2,4,6,-trichlorine-5-methyl pyridine, phosphorus oxychloride an
Pyrimidine derivatives having a herbicidal action and an action regulating plant growth
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, (2008/06/13)
N-Pyrimidin-4-yl-N'-sulfonylureas of the formula I and the basic addition salts thereof have herbicidal properties and properties for regulating, especially inhibiting, plant growth: STR1 the symbols in this formula having the following meanings: Q is hal