Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

136190

Sigma-Aldrich

1-Iodo-2-nitrobenzene

97%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
IC6H4NO2
CAS Number:
609-73-4
Molecular Weight:
249.01
EC Number:
210-200-1
MDL number:
MFCD00007088
UNSPSC Code:
12352100
PubChem Substance ID:
24848264
NACRES:
NA.22

Quality Level

200

assay

97%

form

solid

bp

288-289 °C (lit.)

mp

49-51 °C (lit.)

functional group

iodo
nitro

SMILES string

[O-][N+](=O)c1ccccc1I

InChI

1S/C6H4INO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H

InChI key

JXMZUNPWVXQADG-UHFFFAOYSA-N

Application

1-Iodo-2-nitrobenzene was used in one step synthesis of 2-(2-Pyridyl)-3H-indol-3-one N-Oxide. 1-Iodo-2-nitrobenzene was used in the synthesis of 1-(2-Nitrophenyl)-1H-indole in the presence of PEG3400 (poly(ethylene glycol))–Cs2CO3–copper pre-catalyst under microwave activation.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL8764
BCCH2730
BCCD6164
BCBX5715
BCBT1457

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Dardan Hetemi et al.
Acta chimica Slovenica, dec(4), 818-824 (2018-01-11)
An efficient, versatile and non-destructive in situ method in reaction monitoring using vibrational spectroscopy is described. A Suzuki cross-coupling reaction was monitored in which the substrate 1-iodo-2-nitrobenzene reacted with the electrophile phenylboronic acid to form the product 2-nitrobiphenyl. To hasten
A one-step synthesis of 2-(2-Pyridyl)-3H-indol-3-one N-oxide: is it an efficient spin trap for hydroxyl radical?
G M Rosen et al.
The Journal of organic chemistry, 65(14), 4460-4463 (2000-07-13)
PEG3400-Cs2CO3: an efficient and recyclable microwave-enhanced catalytic system for ligand-free Ullmann arylation of indole and benzimidazole.
Colacino E, et al.
Tetrahedron, 66(21), 3730-3735 (2010)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service