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Chemical Structure| 77-48-5 Chemical Structure| 77-48-5
Chemical Structure| 77-48-5

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1,3-Dibromo-5,5-dimethylhydantoin is an alkyl chain-based PROTAC linker used to synthesize PROTAC molecules.

4.5 *For Research Use Only !

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Product Details of 1,3-Dibromo-5,5-dimethylhydantoin

CAS No. :77-48-5
Formula : C5H6Br2N2O2
M.W : 285.92
SMILES Code : O=C1N(Br)C(C(C)(C)N1Br)=O
MDL No. :MFCD00003189
InChI Key :VRLDVERQJMEPIF-UHFFFAOYSA-N
Pubchem ID :6479

Safety of 1,3-Dibromo-5,5-dimethylhydantoin

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H272-H301-H314-H410
Precautionary Statements:P220-P273-P280-P301+P310-P305+P351+P338-P310
Class:5.1(6.1)
UN#:3087
Packing Group:

Application In Synthesis of 1,3-Dibromo-5,5-dimethylhydantoin

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 77-48-5 ]

[ 77-48-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 59-49-4 ]
  • [ 77-48-5 ]
  • [ 19932-85-5 ]
YieldReaction ConditionsOperation in experiment
With trifluorormethanesulfonic acid; In dichloromethane; ethyl acetate; EXAMPLE 251A 6-bromo-1,3-benzoxazol-2(3H)-one A mixture of 2-benzoxazolinone (3.00 g, 22.2 mmol), 1,3-dibromo-5,5-dimethylhydantoin (3.49 g, 12.2 mmol), and trifluoromethanesulfonic acid (5.00 g, 33.3 mmol) in dichloromethane (100 mL) at room temperature was protected from light, stirred for 1 hour, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 50% ethyl acetate/hexanes to provide the desired product.
With trifluorormethanesulfonic acid; In dichloromethane; ethyl acetate; Example 251A 6-bromo-1,3-benzoxazol-2(3H)-one A mixture of 2-benzoxazolinone (3.00 g, 22.2 mmol), 1,3-dibromo-5,5-dimethylhydantoin (3.49 g, 12.2 mmol), and trifluoromethanesulfonic acid (5.00 g, 33.3 mmol) in dichloromethane (100 mL) at room temperature was protected from light, stirred for 1 hour, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 50% ethyl acetate/hexanes to provide the desired product.
  • 2
  • [ 13708-12-8 ]
  • [ 93-59-4 ]
  • [ 77-48-5 ]
  • [ 131454-80-3 ]
YieldReaction ConditionsOperation in experiment
15.5 parts (100%) In tetrachloromethane; EXAMPLE 1 A mixture of 10 parts of <strong>[13708-12-8]5-methylquinoxaline</strong>, 10 parts of 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione, 1.7 parts of benzenecarboperoxoic acid and 318 parts of tetrachloromethane was stirred for 16 hours at reflux temperature under 2 lamps of 250 Watt. The reaction mixture was cooled and the organic layer was decanted. The product was filtered off and dried, yielding 15.5 parts (100%) of 5-(bromomethyl)quinoxaline (interm. 1).
 

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