| Weight | 226.029 g/mol |
|---|---|
| Formula | C8H4BrNO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Bromoisatin (87-48-9)
5-bromisatin
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- Synthesis, Characterization and Cytotoxic Activity of S-Benzyldithiocarbazate Schiff Bases Derived from 5-Fluoroisatin, 5-Chloroisatin, 5-Bromoisatin and Their Crystal Structures (Journal of Chemical Crystallography, 2011)
- Synthesis of isatin and 5-bromoisatin derivatives (Russian Journal of Organic Chemistry, 2001)
- PROMOTION OF ANALGESIC AND SEDATIVE ACTION WITH 5-BROMOISATIN (1969)
- New Compounds. 5-Ido-7-bromoisatin and 2-Amino-3-bromo-5-idobenzoic Acid (Journal of the American Chemical Society, 1941)
- Studies on heterocyclic compounds: indol-2,3-dione derivatives. IX. 5-Bromoisatin-3-imines. (Bollettino della Societa italiana di biologia sperimentale, 1988)
- Coordination compounds of cobalt(II) and nickel(Il) with the -semicarbazones of isatin and 5-bromoisatin and their antimicrobial activity (Pharmaceutical Chemistry Journal, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-bromisatin
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SMILESC1=CC2=C(C=C1Br)C(=O)C(=O)N2
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InChIKeyMBVCESWADCIXJN-UHFFFAOYSA-N
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