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515396

Sigma-Aldrich

3,5-Dibromobenzaldehyde

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About This Item

Linear Formula:
Br2C6H3CHO
CAS Number:
Molecular Weight:
263.91
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

mp

84-88 °C (lit.)

Quality Level

SMILES string

Brc1cc(Br)cc(C=O)c1

InChI

1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H

InChI key

ZLDMZIXUGCGKMB-UHFFFAOYSA-N

Related Categories

Application

Reactant involved in:
  • Suzuki-Miyaura cross-coupling reactions
  • Synthesis of blue fluorescent dye derivatives for organic light emitting diodes
  • Sharpless kinetic resolution for the formation of Baylis-Hillman enal adducts
  • Synthesis of podophyllotoxin mimetic pyridopyrazoles as anticancer agents
  • Allylic alkylation
  • Synthesis of C2-symmetric biphosphine ligand I

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)

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The preparation and evaluation of novel aryl urea analogs as broad-spectrum antibacterial agents is described. Numerous compounds showed low micromolar minimum inhibitory concentrations (MIC) against both Gram-positive and Gram-negative bacteria. Selected analogs also exhibited in vivo efficacy in a lethal
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Kim CK, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(1), 254-263 (2006)
Conformational Behavior of Conjugated Polymers With Oligo (phenylene vinylene) Side Chains.
Peeter H and Koeckelberghs G.
Macromolecular Chemistry and Physics, 214(5), 538-546 (2013)

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