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Safe transport of cyanamide

Journal of Hazardous Materials, 2009
For many years cyanamide (CAS no. 420-04-2) was not commercially available due to its unstable nature. Since about 1965 the former "Süddeutsche Kalkstickstoffwerke AG" (current name: AlzChem Trostberg GmbH) developed a special stabilizing system. It was to be investigated to which Class (e.g. "Corrosive Substances", Class 8) or Division (e.g.
Thomas Guethner
exaly   +4 more sources

Polycyclotrimerisation of cyanamides

Russian Chemical Reviews, 1989
The results of studies in the field of the synthesis of polymers with a network structure by the polycyclotrimerisation of cyanamides and oligomers containing cyanamide groups are surveyed and analysed. The prospects for the use of polymers based on compounds containing cyanamide groups in the preparation of various thermostable materials are discussed.
A E Chesnokova, V A Pankratov
openaire   +2 more sources

Tautomerism of Cyanamide

Nature, 1944
THE constitution of cyanamide, since its first synthesis in 1851, has been the subject of a very large number of publications. Whereas the chemical properties of this substance point to the structures NH2CN and NH : C : NH, its physical properties are held1 to favour the former.
H. A. Rees, L. Hunter
openaire   +2 more sources

ChemInform Abstract: THE DIMERS OF CYANAMIDE

Chemischer Informationsdienst, 1983
Abstract Ab initio calculations have been performed on various dimeric forms of cyanamide. The “nondissociative” dimerization of cyanamide leads to cyclic molecules all of which are unstable with respect to cyanamide. However, the molecules produced by “dissociative” dimerization are stable relative to cyanamide. Dicyandiamide is found to be the most
openaire   +3 more sources

Determination of Calcium Cyanamide in Crude Calcium Cyanamide

1981
Abstract : A rapid method of analysis for the assay of crude calcium cyanamide is proposed for the monitoring of calcium cyanamide in the nitroguanidine continuous process line. The proposed method consists of (1) micomilling the crude material, (2) extracting the milled material with a sodium acetate/acetic acid buffer, and (3) determining the ...
Charles Ribaudo, Francis X Murphy
openaire   +1 more source

Lattice Vibrations of Molecular Crystals. II. Cyanamide and Cyanamide-d2

The Journal of Chemical Physics, 1968
The far-infrared spectra (33–500 cm−1) of crystalline cyanamide (NH2CN) and cyanamide-d2 have been recorded with polyethylene and silicon sample support plates. The laser Raman spectra have also been recorded from 40–1600 cm−1 for both molecules. No evidence was found for the inversion doubling and resultant low-frequency components of the NH2 and ND2 ...
F. G. Baglin, J. R. Durig, M. Walker
openaire   +2 more sources

Vibrational Spectra and the Inversion Phenomenon in Cyanamide and Deuterated Cyanamide

The Journal of Chemical Physics, 1963
The infrared and Raman spectra of H2NCN and D2NCN have been examined in the liquid state in the region of 2.5 to 35 μ. Polarization data imply a planar configuration, but the experimental data for the region beyond 12 μ are inconsistent with this. The observed product rule ratio for the symmetric N–H stretch, NH2 deformation, N–C and C≡N stretches are ...
Farrell B. Brown, William H. Fletcher
openaire   +2 more sources

The cyanamide–isocyanamide rearrangement

The Journal of Chemical Physics, 1980
A b initio self-consistent field (SCF) and correlated SCEP calculations have been used to study the relative energies and structures of cyanamide, isocyanamide, and the transition state for the rearrangement reaction. Isocyanamide is found to be 53 kcal less stable than cyanamide, larger than the typical isocyanide–cyanide energy difference ...
Mark A. Vincent, Clifford E. Dykstra
openaire   +3 more sources

Copper-Catalyzed Alkenylation of Cyanamides

Organic Letters, 2017
An efficient procedure for the copper-catalyzed cross-coupling between a broad range of cyanamides and iodoalkenes is reported. Upon reaction with catalytic amounts of copper(I) iodide and 2,2'-bisimidazole in the presence of cesium carbonate in DMF at 80 °C, a fast, regioselective, and stereoretentive cross-coupling occurs.
Antoine Nitelet   +3 more
openaire   +4 more sources

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