| Weight | 189.077 g/mol |
|---|---|
| Formula | C6H5BrS |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Bromothiophenol (6320-02-1)
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- Stereoselective Synthesis of Thiochroman-4-ones by Ring Transformation of Chiral 5-Ylidene-1,3-dioxan-4-ones with 2-Bromothiophenol via BromoLithium Exchange (European Journal of Organic Chemistry, 2001)
- Liquid-Liquid Extraction-Spectrophotometric Determination of Vanadium with 2-Hydroxy-5-Bromothiophenol and Aromatic Amines (2015)
- ChemInform Abstract: Stereoselective Synthesis of Thiochroman4ones by Ring Transformation of Chiral 5Ylidene1,3dioxan4ones with 2Bromothiophenol via BromoLithium Exchange. (ChemInform, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C(=C1)S)Br
-
InChIKeyYUQUNWNSQDULTI-UHFFFAOYSA-N
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