| Weight | 277.586 g/mol |
|---|---|
| Formula | C12H9AsClN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
Adamsite (578-94-9)
phenarsazine chloride · 10-chloro-5,10-dihydroarsacridine · diphenylaminochloroarsine
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- Chemistry of the phenoxathiins and isosterically related heterocycles. XX. Assignment of the 13C-NMR spectra of phenarsazine-10-chloride and several substituted analogs. The effect of substitution on the anisotropic reorientation of the phenarsazine system (Journal of Heterocyclic Chemistry, 1982)
- Mass spectrometry of 10chloro5, 10dihydrophenarsazine (adamsite) and 10methyl5, 10dihydrophenarsazine (Journal of Heterocyclic Chemistry, 1966)
- Derivatization of 10-chloro-5,10-dihydrophenarsazine (Adamsite) for gas chromatographic analysis (Journal of Chromatography A, 1996)
- ADAMSITE-(Y), A NEW SODIUM-YTTRIUM CARBONATE MINERAL SPECIES FROM MONT SAINT-HILAIRE, QUEBEC (Canadian Mineralogist, 2000)
- Conversion of adamsite (phenarsarzin chloride) by fungal manganese peroxidase (Applied Microbiology and Biotechnology, 2004)
- Arsenic containing heterocycles. II. Confirmation of the structure of benzo[a]-9-chlorophenarsazine 12-chloride by 13C-NMR spectroscopy and spin-lattice relaxation time studies: Possible evidence for the contribution of an 75as-13C mechanism to the relaxation of the arsenic bearing quarternary carbons in the phenarsazine ring system (Journal of Heterocyclic Chemistry, 1983)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenarsazine chloride
- 10-chloro-5,10-dihydroarsacridine
- diphenylaminochloroarsine
-
SMILESC1=CC=C2C(=C1)NC3=CC=CC=C3[As]2Cl
-
InChIKeyPBNSPNYJYOYWTA-UHFFFAOYSA-N
- Pubchem - Adamsite
- Wikipedia - phenarsazine chloride
Adamsite or DM is an organic compound; technically, an arsenical diphenylaminechlorarsine, that can be used as a riot control agent. DM belongs to the group of chemical warfare agents known as vomiting agents or sneeze gases. First synthesized in Germany by Heinrich Otto Wieland in 1915, it was independently developed by the US chemist Roger Adams (for whom it is named) at the University of Illinois in 1918.
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