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M89625

Sigma-Aldrich

Mucobromic acid

99%

Synonym(s):

2,3-Dibromomalealdehydic acid

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About This Item

Linear Formula:
OHCCBr=CBrCOOH
CAS Number:
488-11-9
Molecular Weight:
257.86
Beilstein:
1705707
EC Number:
207-670-5
MDL number:
MFCD00063745
UNSPSC Code:
12352100
PubChem Substance ID:
24897300
NACRES:
NA.22

Quality Level

100

Assay

99%

form

crystals

mp

120-124 °C (lit.)

SMILES string

OC(=O)\C(Br)=C(\Br)C=O

InChI

1S/C4H2Br2O3/c5-2(1-7)3(6)4(8)9/h1H,(H,8,9)/b3-2-

InChI key

NCNYEGJDGNOYJX-IHWYPQMZSA-N

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Related Categories

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6734
STBK2527
STBJ5824
STBF7290V
STBF1120V

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Ulisses A Pereira et al.
Chemistry & biodiversity, 12(7), 987-1006 (2015-07-15)
Natural phytotoxins and their synthetic analogs are a potential source of new bioactive compounds for agriculture. Analogs of rubrolides, a class of γ-alkylidene-γ-lactones isolated from different ascidians, have been shown to interfere with the photosynthetic electron-transport chain, yet their activity

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