58258-66-5

Basic information

• Product Name: 1-Iodo-4-nitronaphthalene
• Synonyms: 1-Iodo-4-nitronaphthalene
• CAS NO: 58258-66-5
• Molecular Formula: C₁₀H₆INO₂
• Molecular Weight: 299.06461
• Mol File: 58258-66-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Iodo-4-nitronaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Iodo-4-nitronaphthalene(58258-66-5)
• EPA Substance Registry System: 1-Iodo-4-nitronaphthalene(58258-66-5)

Safety Data

• Hazardous Substances Data: 58258-66-5(Hazardous Substances Data)

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

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

Downstream Products

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

Relevant articles and documents

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.

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.

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