| Weight | 285.923 g/mol |
|---|---|
| Formula | C5H6Br2N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,3-Dibromo-5,5-dimethylhydantoin (77-48-5)
1,3-dibromo 5,5-dimethylhydantoin · 2,4-dibromo-5,5-dimethylhydantoin
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- 1,3-DIBROMO-5,5-DIMETHYLHYDANTOIN, A USEFUL REAGENT FOR AROMATIC BROMINATION (Tetrahedron Letters, 1997)
- Halogenation Using N-Halogenocompounds. II. Acid Catalyzed Bromination of Aromatic Compounds with 1,3-Dibromo-5,5-dimethylhydantoin (Bulletin of the Chemical Society of Japan, 1994)
- 1,3-Dibromo-5,5-dimethylhydantoin or N-bromosuccinimide as efficient reagents for chemoselective deprotection of 1,1-diacetates under solvent-free conditions (Monatshefte Fur Chemie, 2009)
- Synthesis of 2-Amino-5-substituted-1,3,4-oxadiazoles Using 1,3-Dibromo-5,5-dimethylhydantoin as Oxidant. (Tetrahedron Letters, 2006)
- gem-Difluorination of 1,3-dithiolanes with the hexafluoropropene-diethylamine reagent and N-iodosuccinimide or 1,3-dibromo-5,5-dimethylhydantoin (Journal of Fluorine Chemistry, 1995)
- Solvent-free Synthesis of 2,4,6-Triarylpyridine Derivatives Promoted by 1,3-Dibromo-5,5-dimethylhydantoin (Organic Preparations and Procedures International, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,3-dibromo 5,5-dimethylhydantoin
- 2,4-dibromo-5,5-dimethylhydantoin
-
SMILESCC1(C(=O)N(C(=O)N1Br)Br)C
-
InChIKeyVRLDVERQJMEPIF-UHFFFAOYSA-N
- Pubchem - 1,3-Dibromo-5,5-dimethylhydantoin
- Wikipedia - 1,3-dibromo-5,5-dimethylhydantoin
DBDMH is an organic compound derived from the heterocycle called dimethylhydantoin. This white crystalline compound with a slight bromine odor is widely used as a disinfectant used for drinking water purification, recreational water treatment, as a bleaching agent in pulp and paper mills, and for treating industrial/commercial water cooling systems. Its action does not involve the use of hypochlorous acid.
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