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488-11-9

Mucobromic acid

CAS: 488-11-9

Molecular Formula: C4H2Br2O3

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488-11-9 - Names and Identifiers

Name Mucobromic acid
Synonyms Bromomucic acid
Mucobromic acid
MUCOBROMIC ACID
Malealdehydic acid, dibromo-
2,3-Dibromomalealdehydic acid
2,3-Dibromo-4-oxo-2-butenoic Acid
3-dibromo-4-oxo-(z)-2-butenoicaci
(Z)-2,3-dibromo-4-oxo-2-butenoate
(2Z)-2,3-dibromo-4-oxobut-2-enoate
(2E)-2,3-dibromo-4-oxobut-2-enoate
(2E)-2,3-dibromo-4-oxobut-2-enoic acid
(2Z)-2,3-dibromo-4-oxobut-2-enoic acid
(2Z)-2,3-Dibromo-4-oxo-2-butenoic acid
2-Butenoic acid, 2,3-dibromo-4-oxo-, (Z)-
Mucobromic acid (2,3-dibromo-4-oxo-2-butenoic acid) (open form)
CAS 488-11-9
EINECS 207-670-5
InChI InChI=1/C4H2Br2O3/c5-2(1-7)3(6)4(8)9/h1H,(H,8,9)/p-1/b3-2+

488-11-9 - Physico-chemical Properties

Molecular FormulaC4H2Br2O3
Molar Mass257.86
Density2.2801 (rough estimate)
Melting Point120-124 °C (lit.)
Boling Point321.8±42.0 °C(Predicted)
Flash Point148.4°C
Solubility methanol: 0.1g/mL, clear
Vapor Presure5.99E-05mmHg at 25°C
AppearanceWhite crystal
ColorWhite to beige
BRN1705707
pKa0.28±0.44(Predicted)
Storage ConditionInert atmosphere,Room Temperature
Refractive Index1.4947 (estimate)
MDLMFCD00063745
Physical and Chemical PropertiesWhite orthogonal crystal. Melting point 125 °c. Soluble in water, alcohol.
UseIs an intermediate in organic synthesis

488-11-9 - Risk and Safety

Risk CodesR34 - Causes burns
R37 - Irritating to the respiratory system
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S27 - Take off immediately all contaminated clothing.
UN IDsUN 3261 8/PG 2
WGK Germany3
TSCAYes
HS Code29183000
Hazard Class8
Packing GroupIII

488-11-9 - Reference Information

NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
Use is an organic synthesis intermediate
Production method Add 2-furanoic acid to water to cool, stir, and add bromine dropwise. The reactants were heated and refluxed for 0.5h. After full cooling, the product is precipitated, filtered, and the filter cake is ground with sodium bisulfite and water before filtering to obtain crude products. The crude product was recrystallized with boiling water and decolorized with activated carbon to obtain pure product 2, 3-dibromo-2-butenal acid. Yield 64-67%.
Last Update:2024-04-10 22:29:15
488-11-9
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View History
488-11-9
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