1959
DOI: 10.1021/ja01519a060
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The Preparation and Reactions of 1-Cyanoformamide

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Cited by 20 publications
(9 citation statements)
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“…These include H2NCN (hydrolyzing first to urea, also valuable, and then to ammonium carbonate) and HCCCN (hydrolyzing first to NCCH2CHO, also valuable). Cyanogen (NCCN) hydrolyzes first to NCCONH2 in weak acidic solution; [95] in base, NCCN hydrolyzes first to HCN and HOCN; [31] various other products are produced by further hydrolysis. All of these would have precipitated to the surface, together with their further hydrolysis products.…”
Section: A Moneta-sized Impact Would Have Opened a Window For Forming...mentioning
confidence: 99%
“…These include H2NCN (hydrolyzing first to urea, also valuable, and then to ammonium carbonate) and HCCCN (hydrolyzing first to NCCH2CHO, also valuable). Cyanogen (NCCN) hydrolyzes first to NCCONH2 in weak acidic solution; [95] in base, NCCN hydrolyzes first to HCN and HOCN; [31] various other products are produced by further hydrolysis. All of these would have precipitated to the surface, together with their further hydrolysis products.…”
Section: A Moneta-sized Impact Would Have Opened a Window For Forming...mentioning
confidence: 99%
“…4.3 g cyanogen (NCCN) were destilled into a stirred mixture of 0.5 g K 2 Cr 2 O 7 in 20 g water and kept at 20°C for 1 h. Unreacted cyanogen and water were destilled off in vacuum and the remaining crystalline cyanoformamide, which melts at 58-60°C [11], was purified by sublimation in vacuum twice. Although slightly unstable, the product could be stored at room temperature and used for investigation over several years.…”
Section: Experimental Aspectsmentioning
confidence: 99%
“…Separation can be accomplished by renewed sublimation yielding colourless, prismatic crystals which slowly turn yellow, when exposed to light or to X-ray radiation. The X-ray structure determination showed this compound to be cyanoformamide (ureamononitrile), formed by monomerization of the starting triazine; this substance, incorporated into tpany insectizides, can be synthesized in very high yield from cyanogen, water, formic acid, and acetonitrile (Welcher et al, 1959). 728 (3) 40(3) 24(2) 0 -1(2) 0 C(2) 0.1281(6) 0.2500 0.4473 (8) 33(3) 42(3) 33(3) 0 -2(2) 0 N(l) 0.3899(5) 0.2500 0.5501 728 (2) 60(3) 24(2) 0 1(2) 0 N(2) 0.0361(7) 0.2500 0.3325 750 (3) 60(4) 43(3) 0 -19(3) 0 0(1) 0.1914(5) 0.2500 0.7603 633 2) 81(3) 26(2 101.4(10) H 20.463(10) 0.250 0.642 113.5 20• The temperature factor T is given by the equation :…”
Section: Introductionmentioning
confidence: 99%