| Weight | 136.976 g/mol |
|---|---|
| Formula | C3H5BrO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Epibromohydrin (3132-64-7)
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- Vibrational spectra and conformations of (bromomethyl)cyclopropane and epibromohydrin (Journal of Raman Spectroscopy, 1982)
- CuII immobilized on guanidinated epibromohydrin functionalized -Fe2O3@TiO2 (-Fe2O3@TiO2-EG-CuII): a novel magnetically recyclable heterogeneous nanocatalyst for the green one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles through alkyneazide cycloaddition in water (RSC Advances, 2016)
- One-Pot Cyclizations of Dilithiated Oximes and Hydrazones with Epibromohydrin. Efficient Synthesis of 6-Hydroxymethyl-5,6-dihydro-4H-1,2-oxazines and Oxazolo[3,4-b]pyridazin-7-ones. (Journal of Organic Chemistry, 2006)
- Chemo-, regio-, and diastereoselective synthesis of functionalized cyclopropanes by cyclization of dilithiated nitriles with epibromohydrin. (Organic Letters, 2001)
- Reaction of dianions of acetoacetic esters with epibromohydrin derivatives: A novel synthesis of tetrahydrofuran derivatives and tetrahydropyran derivatives (Tetrahedron Letters, 1999)
- The reaction of epibromohydrin with hydroxyquinazolin-2-(1H)one derivatives. Novel oxazine formation (Journal of Heterocyclic Chemistry, 1979)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - H311: Toxic in contact with skin
Danger Acute toxicity, dermal - Category 3 -
SMILESC1C(O1)CBr
-
InChIKeyGKIPXFAANLTWBM-UHFFFAOYSA-N
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Epibromohydrin
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