34244-15-0

Basic information

• Product Name: 1-Iodopyrene
• Synonyms: 1-Iodopyrene;Pyrene, 1-iodo-
• CAS NO: 34244-15-0
• Molecular Formula: C₁₆H₉I
• Molecular Weight: 328.14713
• EINECS: -0
• Mol File: 34244-15-0.mol
• Article Data: 8

Chemical Properties

• Melting Point: 89.0 to 93.0 °C
• Appearance: /
• CAS DataBase Reference: 1-Iodopyrene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Iodopyrene(34244-15-0)
• EPA Substance Registry System: 1-Iodopyrene(34244-15-0)

Safety Data

• Hazardous Substances Data: 34244-15-0(Hazardous Substances Data)

Usage

Chemical structure

A pyrene molecule with an iodine atom attached to it.

Reactivity

Highly reactive in organic synthesis and chemical research.

Toxicity

Highly toxic, posing serious health risks to humans and the environment.

Mutagenic properties

Known to be a mutagen, which can cause changes in genetic material.

Carcinogenic properties

Recognized as a carcinogen, potentially leading to cancer development.

Hazard classification

Classified as a hazardous substance due to its harmful effects.

Regulations

Subject to strict regulations on use and disposal to minimize negative impacts on health and the environment.

Upstream product

• 1606-67-3 1-aminopyrene 
• 591-51-5 phenyllithium 
• 1714-29-0 1-bromopyrene 
• 129-00-0 pyrene 
• 74391-90-5 1-pyrenyllithium 

Downstream Products

• 34034-20-3 (1-dihydropyren-3-yl)phenylsulfane 
• 1606-67-3 1-aminopyrene 
• 3443-45-6 1-pyrenebutyric acid 
• 34993-56-1 1-ethynylpyrene 
• 5101-26-8 1,1'-dipyrenyl 
• 102442-84-2 2′-nitrophenyl-1-pyrene 
• 34034-25-8 1-tosylpyrene 

Relevant articles and documents

Sterically driven metal-free oxidation of 2,7-di-tert-butylpyrene

We disclose an unprecedented single-step metal-free green oxidation of 2,7-di-tert-butylpyrene selectively into either the corresponding 4,5-dione or 4,5,9,10-tetraone, two key building blocks used for organic optoelectronic applications using hypervalent

A palladium-catalyzed domino reaction as key step for the synthesis of functionalized aromatic amino acids

A variety of substituted aromatic systems are synthesized by the Catellani reaction. These are used as precursors for novel amino acids with a basic side chain. Georg Thieme Verlag Stuttgart New York.

Pyrene-fused porphyrins: Annulation reactions of meso-pyrenylporphyrins

We prepared novel pyrene-fused porphyrins via the oxidative intramolecular ring closure reactions of meso-pyrenylporphyrin. The excitation energies and the oxidation potentials of the isolated dark-colored pyrene-fused porphyrins were significantly low compared with those of the corresponding precursors.