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4-Nitro-2,6-dibromophenol

2,6-dibromo-4-nitrophenol

CAS: 99-28-5

Molecular Formula: C6H3Br2NO3

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4-Nitro-2,6-dibromophenol - Names and Identifiers

Name 2,6-dibromo-4-nitrophenol
Synonyms NSC 2585
AI3-01539
BRN 1245050
2,6-DibroMo-4-nitrop
2,6-dibromo-4-nitrophenol
4-Nitro-2,6-dibromophenol
2,6-dibromo-4-nitro-pheno
2,6-Dibromo-4-nitrophenol
2,6-Dibromo-4-mitrophenol
2,6-DIBROMO-4-NITROPHENOL
Dibromo-4-nitrophenol, 2,6-
Phenol, 2,6-dibromo-4-nitro-
2,6-dibromo-4-nitrophenolate
4-06-00-01366 (Beilstein Handbook Reference)
CAS 99-28-5
EINECS 202-744-3
InChI InChI=1/C6H3Br2NO3/c7-4-1-3(9(11)12)2-5(8)6(4)10/h1-2,10H/p-1
InChIKey WBHYZUAQCSHXCT-UHFFFAOYSA-N

4-Nitro-2,6-dibromophenol - Physico-chemical Properties

Molecular FormulaC6H3Br2NO3
Molar Mass296.9
Density2.3436 (rough estimate)
Melting Point145°C (dec.)(lit.)
Boling Point297.8±40.0 °C(Predicted)
Flash Point133.9°C
Vapor Presure0.000744mmHg at 25°C
Appearancepowder to crystal
ColorWhite to Orange to Green
BRN1245050
pKa3.67±0.44(Predicted)
Storage Condition2-8°C(protect from light)
Refractive Index1.6220 (estimate)
MDLMFCD00007334
Physical and Chemical PropertiesYellow columnar crystals. Melting point of 144 deg C, above 144 deg C decomposition. Soluble in ether, carbon disulfide, ethyl acetate, chloroform and hot alcohol, difficult to dissolve in benzene, acetic acid and petroleum ether, almost insoluble in water. Can volatilize with water vapor.

4-Nitro-2,6-dibromophenol - Risk and Safety

Risk CodesR20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S37 - Wear suitable gloves.
WGK Germany3
RTECSSK8025000
TSCAYes
HS Code29089990

4-Nitro-2,6-dibromophenol - Reference Information

NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Use as an intermediate in organic synthesis.
production method obtained by bromination of p-nitrophenol. P-nitrophenol and glacial acetic acid were mixed and then stirred to dissolve all of them. A mixed solution of bromine and glacial acetic acid was slowly added at 20-25 ° C. For about 3 hours, and then stirred for 1 hour and kept at 85 ° C. For 1 hour. The bromine was condensed by pressure, precipitated by stirring with water, cooled for 6h, filtered, and the crystals were washed with 50% acetic acid, then washed with water and dried at 40-60 °c to give a crude product. The product was then recrystallized from acetic acid.
Last Update:2024-04-09 21:01:54
4-Nitro-2,6-dibromophenol
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