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- KODAMA Yutaka
- 富山化学工業株式会社開発部
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- SEKIBA Tetuya
- 富山化学工業株式会社開発部
Bibliographic Information
- Other Title
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- クロルシアンの四量体およびその誘導体に関する研究(第3報)
- クロルシアン ノ ヨンリョウタイ オヨビ ソノ ユウドウタイ ニ カンスル ケンキュウ 3
- Syntheses of 2, 4-dichloro-6-isocyanate-s-triazine
- 2,4-ジクロロ-6-イソシアナート-s-トリアジンの製造法
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Description
Thermal decomposition of 2, 4-dichloro-6-a koxychloroisocyano-s-triazine, derived from chlorocyan tetramer (2, 4-dichloro-6-isocyanodichloro-s-triazine) above 140°c caused liberation of alkyl chloride easily and gave 2, 4-dichloro-6-isocyanate-striazine. This iso-cyanate was extremely unstable in the atmospheric moisture and decomposed immediately to 2, 4-dichloro-6-amino-s-triazine. The identification of this isocyanate was carried out by the following three methods : 1. Urethane was formed by the reaction with alcohol, 2. hydrolysis of 1 mol isocyanate gave 1 mol of ammelide, 1 mol carbon dioxide and two atoms of chlorine, and 3. infrared absorption spectra indicated the max. absorptions at 2, 260 cm-1 - 2200 cm-1 characteristic of isocyanate group.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 21 (11), 888-890, 1963
The Society of Synthetic Organic Chemistry, Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390282680288093824
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- NII Article ID
- 130000923221
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- NII Book ID
- AN0024521X
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- ISSN
- 18836526
- 00379980
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- NDL BIB ID
- 9213667
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed