2-Iodo-4-nitrotoluene, 97%

Name: 2-Iodo-4-nitrotoluene, 97% | 7745-92-8
Brand: J&K Chemical
SKU: JK561516_5_G
Price: 61.8 USD
Availability: InStock

Cat. No JK561516_5_G

Vendor: J&K Chemical

Product Information

Product Name

2-Iodo-4-nitrotoluene, 97%

Brand Name

J&K

Product Number

561516

CAS

7745-92-8

Molecular Formula

C7H6INO2

Molecular Weight

263.03

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

82188

IUPAC Name

2-iodo-1-methyl-4-nitrobenzene

InChI Key

BUQSRXQJUZTIEW-UHFFFAOYSA-N

SMILES

CC1=C(C=C(C=C1)N+(=O)O-)I

Properties

Melting Point

Boiling Point

165

n20D

1.5240

Safety Information

Signal Word

Warning

Hazard Statement

H315

H319

H335

Precautionary Statement

P280

P321

P261

P271

P319

P405

P501

P302+P352

P332+P317

P362+P364

P264+P265

P305+P351+P338

P337+P317

P304+P340

P403+P233

References Data Source From Pubchem

Palladium(0)-Mediated Cyclization with Concomitant Introduction of a 3-Aryl Substituent

Publication Name: Science of Synthesis

Publication Date: 2016

Facile iodination of aromatic compounds having electron-withdrawing substituents. Generation of triiodine cation in the system tetra-N-iodoglycoluril-iodine-sulfuric acid

Publication Name: Russian Journal of Organic Chemistry

Publication Date: 2008-06

DOI: 10.1134/s1070428008060286

Superactivity and dual reactivity of the system N-iodosuccinimide-H2SO4 in the iodination of deactivated arenes

Publication Name: Russian Journal of Organic Chemistry

Publication Date: 2007-09

DOI: 10.1134/s1070428007090035

1,3-Diiodo-5,5-dimethylhydantoin—An efficient reagent for iodination of aromatic compounds

Publication Name: Russian Journal of Organic Chemistry

Publication Date: 2007-09

DOI: 10.1134/s1070428007090060

Reductive Carbonylation of Iodoarenes Using Acetic Formic Anhydride as a Carbon Monoxide Source

Publication Name: Science of Synthesis

Publication Date: 2007

2-Iodo-4-nitrotoluene, 97%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Palladium(0)-Mediated Cyclization with Concomitant Introduction of a 3-Aryl Substituent

Facile iodination of aromatic compounds having electron-withdrawing substituents. Generation of triiodine cation in the system tetra-N-iodoglycoluril-iodine-sulfuric acid

Superactivity and dual reactivity of the system N-iodosuccinimide-H2SO4 in the iodination of deactivated arenes

1,3-Diiodo-5,5-dimethylhydantoin—An efficient reagent for iodination of aromatic compounds

Reductive Carbonylation of Iodoarenes Using Acetic Formic Anhydride as a Carbon Monoxide Source