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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-(2-Iodo-4-nitrophenyl)acetic Acid

OC(=O)Cc1ccc(cc1I)[N+](=O)[O-] Request for Quotation
Chemical Name: 2-(2-Iodo-4-nitrophenyl)acetic Acid
CAS Number: 66949-41-5
Product Number: AG00IBNU(AGN-PC-0WAIID)
Synonyms:
MDL No:
Molecular Formula: C8H6INO4
Molecular Weight: 307.0420

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


With a molecular formula of C8H6INO4, 2-(2-Iodo-4-nitrophenyl)acetic Acid is a powerful reagent widely utilized in chemical synthesis. Its unique structure and properties make it a valuable tool in organic chemistry, particularly in the following applications:1. **Cross-Coupling Reactions:** 2-(2-Iodo-4-nitrophenyl)acetic Acid can be used as a versatile building block in various cross-coupling reactions, such as Suzuki-Miyaura coupling and Heck reaction. By functionalizing the iodo group, researchers can easily introduce diverse substituents and create structurally complex molecules.2. **Medicinal Chemistry:** The nitro and iodo groups in the molecule make it a promising candidate for medicinal chemistry research. These pharmacophores can be selectively modified to design novel drug candidates with improved pharmacological properties and target specificity.3. **Material Science:** In the field of material science, 2-(2-Iodo-4-nitrophenyl)acetic Acid can serve as a precursor for the synthesis of advanced materials, such as polymers, liquid crystals, and conjugated organic compounds. Its structural flexibility allows for tailored modifications to achieve desired material properties.4. **Photophysical Studies:** Researchers also utilize this compound in photophysical studies due to its potential applications in fluorescence imaging, photodynamic therapy, and luminescent materials. The electron-donating and accepting moieties make it a promising fluorophore in bioimaging applications.5. **Natural Product Synthesis:** Chemists often employ 2-(2-Iodo-4-nitrophenyl)acetic Acid in the total synthesis of natural products. Its strategic incorporation into key intermediates enables efficient access to complex natural compounds with diverse biological activities.By leveraging the unique reactivity and functional groups present in 2-(2-Iodo-4-nitrophenyl)acetic Acid, chemists can achieve intricate molecular transformations and drive innovation in various fields of chemical research and development.