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144495

Sigma-Aldrich

1-Iodo-3-nitrobenzene

99%

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About This Item

Linear Formula:
IC6H4NO2
CAS Number:
645-00-1
Molecular Weight:
249.01
EC Number:
211-427-9
MDL number:
MFCD00007218
UNSPSC Code:
12352100
PubChem Substance ID:
24848660
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

Assay

99%

form

solid

bp

280 °C (lit.)

mp

36-38 °C (lit.)

functional group

iodo
nitro

SMILES string

[O-][N+](=O)c1cccc(I)c1

InChI

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

InChI key

CBYAZOKPJYBCHE-UHFFFAOYSA-N

Application

1-Iodo-3-nitrobenzene was used in the synthesis of 5-substituted pyrrolo[3,2-b]pyridine amide[1] and 3′-nitro-4-methylthiobiphenyl[2]. It was used in palladium(0) catalyzed cross-coupling reaction between heteroarylzinc iodide and unsaturated iodide[3].

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

4.1B - Flammable solid 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

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Certificates of Analysis (COA)

Lot/Batch Number
STBK9410
STBG0992V
S41250
15523ME
03818KE

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Hee Jin Kim et al.
Bioorganic & medicinal chemistry letters, 20(1), 413-417 (2009-11-10)
Synthesis of a new series of diarylureas and amides having pyrrolo[3,2-b]pyridine scaffold is described. Their in vitro antiproliferative activity against human melanoma cell line A375 and HS 27 human fibroblast cell line was tested and the effect of substituents on
Preparation and reactions of new zincated nitrogen-containing heterocycles.
Bhanu PAS, et al.
Tetrahedron, 53(21), 7237-7254 (1997)
Rupa Hiremath et al.
Chemical communications (Cambridge, England), (23)(23), 2676-2677 (2004-11-30)
Orthorhombic and triclinic crystals of 2-iodo-4-nitroaniline (INA) grow concomitantly from supersaturated ethanol solutions, but the less stable orthorhombic phase can be selectively grown on 3'-X-4-mercaptobiphenyl (X = NO(2), I) self-assembled monolayer templates.

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