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Key Documents

523151

Sigma-Aldrich

4-Bromo-3-nitrobenzaldehyde

97%

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About This Item

Linear Formula:
BrC6H3(NO2)CHO
CAS Number:
Molecular Weight:
230.02
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

104-108 °C (lit.)

SMILES string

[O-][N+](=O)c1cc(C=O)ccc1Br

InChI

1S/C7H4BrNO3/c8-6-2-1-5(4-10)3-7(6)9(11)12/h1-4H

InChI key

SAFSVELFSYQXOV-UHFFFAOYSA-N

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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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Chunyan Du et al.
The Journal of organic chemistry, 74(19), 7322-7327 (2009-08-29)
Two asymmetrically substituted dicyanovinyl heterotetracenes are synthesized and characterized. Single-crystal X-ray diffractions indicate both intermolecular hydrogen bonds and pi-stacking existing in the solid-state structures. The solvatochromic behaviors of the two heterotetracenes were investigated in a variety of solvents. Both experimental
Jian-Bo Wang et al.
Chemical communications (Cambridge, England), 48(5), 744-746 (2011-11-29)
A novel fluorescent probe for gold ions (Au(3+)/Au(+)) is reported through blocking photoinduced electron transfer, in which a boron dipyrromethene (Bodipy) derivative reveals high selectivity and sensitivity in a gold-catalyzed intramolecular hydroamination, and is successfully applied to fluorescence imaging of
Synthesis and characterization of a conjugated polymer with stable radicals in the side groups.
Swoboda P, et al.
Macromolecules, 28(12), 4255-4259 (1995)

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