Home Halogens 1,3-Dibromo-5,5-dimethylimidazolidine-2,4-dione

1,3-Dibromo-5,5-dimethylimidazolidine-2,4-dione

CAS No.:
77-48-5
Catalog Number:
AG003DJ3
Molecular Formula:
C5H6Br2N2O2
Molecular Weight:
285.9213
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25g
95%
In Stock USA
United States
$33
- +
100g
95%
In Stock USA
United States
$47
- +
500g
95%
In Stock USA
United States
$68
- +
Product Description
Catalog Number:
AG003DJ3
Chemical Name:
1,3-Dibromo-5,5-dimethylimidazolidine-2,4-dione
CAS Number:
77-48-5
Molecular Formula:
C5H6Br2N2O2
Molecular Weight:
285.9213
MDL Number:
MFCD00003189
IUPAC Name:
1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione
InChI:
InChI=1S/C5H6Br2N2O2/c1-5(2)3(10)8(6)4(11)9(5)7/h1-2H3
InChI Key:
VRLDVERQJMEPIF-UHFFFAOYSA-N
SMILES:
BrN1C(=O)N(C(C1=O)(C)C)Br
EC Number:
201-030-9
UNII:
V9R5F9I7MZ
NSC Number:
33305
Properties
Complexity:
229  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
285.878g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
285.923g/mol
Monoisotopic Mass:
283.88g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
40.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5  
Literature
Title Journal
Intramolecular alkene electrophilic bromination initiated ipso-bromocyclization for the synthesis of functionalized azaspirocyclohexadienones. Organic letters 20120706
C3-symmetric trisimidazoline-catalyzed enantioselective bromolactonization of internal alkenoic acids. Chemistry (Weinheim an der Bergstrasse, Germany) 20120702
Organocatalysis as a safe practical method for the stereospecific dibromination of unsaturated compounds. Organic letters 20120406
Synthesis of geminal difluorides by oxidative desulfurization-difluorination of alkyl aryl thioethers with halonium electrophiles in the presence of fluorinating reagents and its application for 18F-radiolabeling. The Journal of organic chemistry 20100917
Effectiveness of 1,3-dibromo-5,5 dimethylhydantoin on reduction of Escherichia coli O157:H7- and Salmonella-inoculated fresh meat. Journal of food protection 20090101
Lewis acid catalyzed benzylic bromination. Chemistry, an Asian journal 20080901
Short intermolecular N-Br...O=C contacts in 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione. Acta crystallographica. Section C, Crystal structure communications 20070701
Quantification of dibromodimethylhydantoin disinfectants in water by chemiluminescent method. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20070301
An efficient, stereoselective synthesis of the hydroxyethylene dipeptide isostere core for the HIV protease inhibitor A-792611. The Journal of organic chemistry 20060707
An efficient chemoenzymatic approach to (S)-gamma-fluoroleucine ethyl ester. The Journal of organic chemistry 20050318
Facile exchange of glycosyl S,S-acetals to their O,O-acetals and preparation of glycofuranosides from acyclic glycosyl S,S-acetals under metal-free reaction conditions in the presence of 1,3-dibromo-5,5-dimethylhydantoin. Carbohydrate research 20050227
Highly efficient catalytic aerobic oxidations of benzylic alcohols in water. The Journal of organic chemistry 20050121
Determination of iodine values using 1,3-dibromo-5,5-dimethylhydantoin (DBH) and ethyl acetate as solvent. Analytical methods with DBH in respect to environmental and economical concern, part 18. Die Pharmazie 20040801
Cetylpyridinium tetrachlorozincate as standard for tenside titration. Analytical methods with 1,3-dibromo-5,5-dimethylhydantoin (DBH) in respect to environmental and economical concern, part 19. Die Pharmazie 20040801
Hypohalites and related oxidants as chemiluminescence reagents: a review. Luminescence : the journal of biological and chemical luminescence 20040101
Synthesis of fluorinated analogs of myristic acid as potential inhibitors of Egyptian armyworm (Spodoptera littoralis) delta11 desaturase. Lipids 20030801
Determination of iodine values using 1,3-dibromo-5,5-dimethylhydantoin (DBH) without the employment of chlorinated hydrocarbons. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern. Part 17. Die Pharmazie 20020801
Determination of organically bound iodine by reductive mineralization with aluminium powder. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern. Part 16. Die Pharmazie 20020701
1,3-Dibromo-5,5-dimethylhydantoin (DBH) as oxidant and precipitant for drug identification according to PH. EUR Analytical methods of pharmacopoeias with DBH in respect of environmental and economical concern, Part 15(1). Die Pharmazie 20020601
Application of 1,3-dibromo-5,5-dimethylhydantoin (DBH) instead of bromine gas or bromine water decolorization for drug identification according to PH. EUR. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 14. Die Pharmazie 20020501
Determination of propylthiouracil using 1,3-dibromo-5,5-dimethylhydantoin (DBH): analytical methods of pharmacopeias with DBH in respect to environmental and economical concern: part 9. Journal of pharmaceutical and biomedical analysis 20020415
Determination of selenium sulfide using 1,3-dibromo-5,5-dimethylhydantoin (DBH). Analytical methods of pharmacopeias with DBH in respect to environmental and economical concern Part 11. Journal of pharmaceutical and biomedical analysis 20020415
Determination of iodine values according to Hanus using 1,3-dibromo-5,5-dimethylhydantoin (DBH): analytical methods of pharmacopeias with DBH: part 7. Journal of pharmaceutical and biomedical analysis 20020401
Replacement of cyanogen bromide solution PH. EUR. with 1,3-dibromo-5,5-dimethylhydantoin (DBH). Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 13. Die Pharmazie 20020401
Colour reactions of PH. EUR. for identification of drugs using 1,3-dibromo-5,5-dimethylhydantoin (DBH) instead of elemental bromine. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 10. Die Pharmazie 20020301
Determination of iron limiting values according to PH. EUR. using 1,3-dibromo-5,5-dimethylhydantoin (DBH) instead of elemental bromine. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern. Part 8. Die Pharmazie 20020101
Determination of phenol and resorcinol using 1,3-dibromo-5,5-dimethylhydantoin (DBH) analogous to the Koppeschaar reaction. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 6. Die Pharmazie 20011001
Identification of lactate. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 4. Die Pharmazie 20010701
Determination of iodide with 1,3-dibromo-5,5-dimethylhydantoin (DBH) in comparison with the ICl-method. Analytical methods of pharmacopeias with DBH in respect to environmental and economical concern. Part 3. Journal of pharmaceutical and biomedical analysis 20010601
Properties