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Key Documents

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:
Molecular Weight:
257.86
Beilstein/REAXYS Number:
1705707
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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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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