| Weight | 222.934 g/mol |
|---|---|
| Formula | C6H5AsCl2 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Dichlorophenylarsine (696-28-6)
phenyldichloroarsine
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- Stress protein synthesis in human keratinocytes treated with sodium arsenite, phenyldichloroarsine, and nitrogen mustard (Toxicological Sciences, 1990)
- One-dimensional and two-dimensional nuclear magnetic resonance studies of the reaction of phenyldichloroarsine with glutathione (Archives of Biochemistry and Biophysics, 1987)
- The interaction of phenyldichloroarsine with erythrocytes. (Journal of Biochemical Toxicology, 1989)
- Spin-echo NMR investigation of the interaction of phenyldichloroarsine with glutathione in intact erythrocytes (Inorganica Chimica Acta, 1987)
- 2D NMR studies of the phenyldichloroarsinebritish antilewisite adduct (Magnetic Resonance in Chemistry, 1987)
- The reaction products of phenyldichloroarsine and acetylene. (Journal of the American Chemical Society, 1947)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenyldichloroarsine
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SMILESC1=CC=C(C=C1)[As](Cl)Cl
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InChIKeyUDHDFEGCOJAVRE-UHFFFAOYSA-N
- Pubchem - Dichlorophenylarsine
- Wikipedia - dichlorophenylarsine
Phenyldichloroarsine, NATO abbreviation PD, is an organic arsenical vesicant and vomiting agent developed by Germany and France for use as a chemical warfare agent during World War I. The agent is known by multiple synonyms and is technically classified as a vesicant, or blister agent.
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