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・ Diphenyl carbonate
・ Diphenyl diselenide
・ Diphenyl disulfide
・ Diphenyl ditelluride
・ Diphenyl ether
・ Diphenyl oxalate
・ Diphenyl sulfone
・ Diphenyl-2-pyridylmethane
・ Diphenyl-2-pyridylphosphine
・ Diphenylacetylene
・ Diphenylalanine
・ Diphenylamine
・ Diphenylamine (data page)
・ Diphenylbutylpiperidine
・ Diphenylchlorarsine
Diphenylcyanoarsine
・ Diphenylcyclopropenone
・ Diphenyldichloromethane
・ Diphenylethylenediamine
・ Diphenylhexatriene
・ Diphenylketene
・ Diphenylmercury
・ Diphenylmethane
・ Diphenylmethanol
・ Diphenylmethylpiperazine
・ Diphenylphosphine
・ Diphenylphosphoryl azide
・ Diphenylprolinol
・ Diphenylpropylamine
・ Diphenylpyraline


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Diphenylcyanoarsine : ウィキペディア英語版
Diphenylcyanoarsine

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Diphenylcyanoarsine, also called Clark 2 (Chlor-Arsen-Kampfstoff 2, being the successor of Clark 1) by the Germans, was discovered in 1918 by Sturniolo and Bellinzoni〔Sturniolo, G. und Bellinzoni , G. (1919); ''Boll. chim. pharm.'', 58, 409–410〕 and shortly thereafter used like the related Clark 1 gas by the Germans for chemical warfare in the First World War. The substance forms colourless, garlic-smelling crystals and causes nausea, vomiting and headaches. It can subsequently lead to e.g. pulmonary oedema (fluid on the lungs).
== See also ==

*Clark 1
*Chemical weapons

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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