Skip to Content
Merck
CN
All Photos(3)

Documents

Safety Information

576689

Sigma-Aldrich

2-Iodo-4-nitroaniline

97%

Sign Into View Organizational & Contract Pricing

Linear Formula:
IC6H3(NO2)NH2
CAS Number:
Molecular Weight:
264.02
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

105-109 °C (lit.)

SMILES string

Nc1ccc(cc1I)[N+]([O-])=O

InChI

1S/C6H5IN2O2/c7-5-3-4(9(10)11)1-2-6(5)8/h1-3H,8H2

InChI key

LOLSEMNGXKAZBZ-UHFFFAOYSA-N

General description

2-Iodo-4-nitroaniline can be synthesized via reaction of 4-nitroaniline with iodine and silver acetate.

Application

2-iodo-4-nitroaniline may be used to synthesize the following:
  • 2-iodo-4-nitrobenzonitrile via reaction with sodium nitrite to form a diazonium salt, which then reacts with a mixture of CuCN/KCN
  • 2-iodo-p-phenylenediamine by reacting with tin(II)dihydrate in conc.HCl

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

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’.

Already Own This Product?

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

Visit the Document Library

"Identification and optimization of a novel series of [2.2. 1]-oxabicyclo imide-based androgen receptor antagonists"
Salvati.EM, et al.
Bioorganic & Medicinal Chemistry Letters, 18(06), 1910-1915 (2008)
"Synthesis of optically active ring-A substituted tryptophans as IDO inhibitors"
Li X, et al.
Tetrahedron Letters, 45(46), 8569-8573 (2004)
"Preparation of 2-arylated-1, 4-phenylenediamines by palladium-catalyzed cross-coupling reactions"
Jensen EA, et al.
Journal of Organometallic Chemistry, 653(01), 122-128 (2002)

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