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| CAS番号. | 92-84-2 |
| 化学名: | フェノチアジン |
| 别名: | フェノチアジン;ヘルメチナ;コンタベルム;オリモン;パドフェン;フェノベルム;レテルミン;10H-フェノチアジン;ネマジン;フェンチアジン;チオジフェニルアミン;レコノックス;ソウフラミン;ビベルム;ジベンゾチアジン;フェネジック;アンチベルム;AFI-チアジン;フェノビス;フェノクスール |
| 英語化学名: | Phenothiazine |
| 英語别名: | ent38;Feeno;XL-50;Biverm;ENT 38;Orimon;Reconox;PHENOXUR;VERMITIN;Antiverm |
| CBNumber: | CB2272320 |
| 分子式: | C12H9NS |
| 分子量: | 199.27 |
| MOL File: | 92-84-2.mol |
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| フェノチアジン 物理性質 |
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| Sensitive : |
Light Sensitive |
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| 安定性：: |
Stable. Combustible. Incompatible with strong oxidizing agents, strong acids. May discolour upon exposure to light. |
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フェノチアジン 化学特性,用途語,生産方法 |
化学的特性
yellow or pale green powder |
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使用
A key component of antipsychotic and antihistaminic drugs. |
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使用
Employed in the preparation of carbazoles and piperazines,1 and charge-transfer semiconducting complexes.2 |
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一般的な説明
Light green to steel-blue powder. Acquires a greenish-brown tint under exposure to sunlight. |
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空気と水の反応
Insoluble in water. |
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反応プロフィール
Phenothiazine is slowly decomposed by sunlight. . Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. |
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火災危険
Flash point data for Phenothiazine are not available, but Phenothiazine is probably combustible. |
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| フェノチアジン 生産企業 Global( 207)Suppliers |
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