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Usage

Derivative of naphthalene

Naphthalene is a common aromatic hydrocarbon, and 1-Iodo-4-nitronaphthalene is a derivative of it, with a nitro group and an iodine atom attached to its carbon ring.

Use in organic synthesis

1-Iodo-4-nitronaphthalene is commonly used in organic synthesis as a building block for producing various pharmaceuticals, agrochemicals, and dyes.

Utilization in research and development

1-Iodo-4-nitronaphthalene is also utilized in the research and development of novel materials and chemical processes.

Classification as hazardous material

1-Iodo-4-nitronaphthalene is classified as a hazardous material, and should be handled with caution due to its potential health and environmental risks.

Upstream product

• 86-57-7 1-Nitronaphthalene 
• 6921-26-2 1,4-dinitronaphthalene 
• 91-20-3 naphthalene 
• 776-34-1 1-amino-4-nitronaphthalene 

Downstream Products

• 36316-83-3 1,4-diiodonaphthalene 
• 200880-19-9 1-(2-carboxy-4,6-dinitrophenyl)-4-nitronaphthalene 
• 200880-17-7 1-(2-carboxy-4-nitrophenyl)-4-nitronaphthalene 
• 200880-18-8 1-(2-carboxy-6-nitrophenyl)-4-nitronaphthalene 
• 200880-13-3 1-(2-carboxyphenyl)-4-nitronaphthalene 
• 17117-34-9 3-nitrobenzanthrone 
• 857953-38-9 acetic acid-[4-(4-nitro-[1]naphthylsulfanyl)-anilide] 

Relevant academic research and scientific papers

Direct cyanation of picolinamides using K4[Fe(CN)6] as the cyanide source

The efficient, simple, and environment-friendly route of direct cyanation of picolinamides has been developed with nontoxic K4[Fe(CN)6] as the cyanide source through Pdcatalyzed C-H bond activation. A series of N-(naphthalene-1- yl)picolinamide derivatives were successfully transformed to the corresponding cyanation products. The cyanation mechanism has also been speculated.

FUSED BENZENE DERIVATIVE AND USE

The present invention provides a compound represented by the general formula: [wherein Ring A represents an optionally substituted 5- to 8-membered ring, Ring B represents a further optionally substituted 4- to 10-membered ring, Ring C represents a further optionally substituted benzene ring, X1 represents carbon atom, X2 represents a carbon atom, an oxygen atom, etc., W represents a nitrogen atom, etc., Y11 represents a group represented by the formula CR2R3' (wherein R2 represents a hydrogen atom, a cyano group, a nitro group, etc., and R3' represents a hydrogen atom, a cyano group, a nitro group, etc., respectively), Y21 represents a group represented by the formula CR4R5' (wherein R4 represents a hydrogen atom, a cyano group, a nitro group, etc., and R5' represents a hydrogen atom, a cyano group, a nitro group, etc., respectively), etc., and R1 represents an electron-withdrawing group, respectively. The formula represents a single bond or a double bond] or a salt thereof, which is useful as an androgen receptor modulator.

Nitrogen dioxide - Sodium iodide as an efficient reagent for the one- pot conversion of aryl amines to aryl iodides under nonaqueous conditions

Successive treatment of aromatic amines with liquid nitrogen dioxide and powdered sodium iodide in acetonitrile at -20 °C, followed by usual work- up, gave the corresponding aryl iodides in good yield. This method worked especially well for less basic amines bearing electron-withdrawing substituents.

The Decomposition of Arenediazonium Tetrafluoroborates with Halo- and Azidotrimethylsilanes in Nonaqueous Solvents

The reaction of arenediazonium tetrafluoroborates with chlorotrimethylsilane in a tetrahydrofuran/N,N-dimethylformamide (DMF) (5v/3v) solution afforded the protodediazotization products in high yields.The reactions of the diazonium salts with halotrimethylsilanes in DMF were found to give the corresponding haloarenes.Among the halodediazotization reactions, the iododediazotization with iodotrimethylsilane proceeded smoothly at room temperature to give the iodoarenes in excellent yields.In a similar manner, a variety of azidoarenes were obtained in cosistently high yields by the treatment of arenediazonium tetrafluoroborates with azidotrimethylsilane in a DMF solution.

SYNTHESIS OF ACETYLENIC COMPOUNDS AND BIS-α-DIKETONES ON THE BASIS OFR ACENAPHTHENE AND NAPHTHALENE DIIODIDES

The direct iodination of acenaphthene by the I2-HIO4 system and of naphthalene in the presence of a nitrating mixture was investigated.The direct synthesis of 2,4-diiodoacenaphthene was realized.The diiodination of naphhtalene by the iodine-nitrating mixt