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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:
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

Signal Word

Danger

Hazard Statements

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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