| Weight | 189.077 g/mol |
|---|---|
| Formula | C6H5BrS |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
4-Bromothiophenol (106-53-6)
p-bromobenzenethiol
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LabBot
- Electrophilic properties of patulin. Adduct structures and reaction pathways with 4-bromothiophenol and other model nucleophiles. (Chemical Research in Toxicology, 2000)
- 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)
- On the thiol-reactivity of patulin: adduct structures and reaction pathways with the thiol model compound 4-bromothiophenol (Revue De Medecine Veterinaire, 1998)
- [Sur la reactivite de la patuline au thiol: structures des adduits et voies de reaction avec le 4-bromothiophenol compose modele thiol] (1998)
- 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. - p-bromobenzenethiol
-
SMILESC1=CC(=CC=C1S)Br
-
InChIKeyFTBCOQFMQSTCQQ-UHFFFAOYSA-N
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