116632-14-5

Basic information

• Product Name: 2-Amino-3-iodonaphthalene
• Synonyms: 2-Amino-3-iodonaphthalene;3-iodonaphthalen-2-amine
• CAS NO: 116632-14-5
• Molecular Formula: C₁₀H₈IN
• Molecular Weight: 269.08
• Mol File: 116632-14-5.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-Amino-3-iodonaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-3-iodonaphthalene(116632-14-5)
• EPA Substance Registry System: 2-Amino-3-iodonaphthalene(116632-14-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 116632-14-5(Hazardous Substances Data)

Usage

General Description

2-Amino-3-iodonaphthalene, also known as 3-Iodo-2-aminonaphthalene, is a chemical compound that contains an amino group and an iodine atom attached to a naphthalene ring. It is primarily used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It can also be utilized as a dye precursor and in the manufacture of other organic compounds. Additionally, it has been studied for its potential applications in various fields, including fluorescence labeling and medicinal chemistry. However, 2-Amino-3-iodonaphthalene is also considered a hazardous material due to its toxic and irritant properties, and proper handling and disposal procedures should be followed to prevent adverse effects on health and the environment.

Upstream product

• 581-89-5 2-nitronaphthalene 
• 93-09-4 naphthalene-2-carboxylate 
• 454713-45-2 naphthalen-2-yl-carbamic acid tert-butyl ester 
• 91-59-8 naphthalen-2-ylamine 
• 5959-52-4 2-Amino-3-naphthoic acid 
• 63212-42-0 3-iodo-2-naphthoic acid 
• 102153-71-9 2-iodo-3-nitronaphthalene 
• 67116-33-0 2-bromo-3-nitronaphthalene 

Downstream Products

• 103027-41-4 1-(tert-butyldimethylsilyl)-4-(4',4',5',5'-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-5-ol 
• 19029-32-4 5,12-dihydro-5,12-diazatetracene 
• 1291080-93-7 3-(dibenzylamino)-2-naphthaldehyde 
• 91820-26-7 2-chloronaphtho[2,3-d]thiazole 
• 39608-20-3 naphtho[2,3-d]thiazole-2-amine 

Relevant articles and documents

Reaction of 2-naphthylamine with sodium iodate/sodium sulfite: Synthesis of 2-amino-1-iodonaphthalene

The reaction of 2-naphthylamine with NaIO3/Na2SO 3/HCl yields exclusively 2-amino-1-iodonaphthalene and not regioisomer 2-amino-3-iodonaphthalene as was previously reported. The assigned structure is supported by spectroscopic data. Taylor & Francis Group, LLC.

Fluorene-containing organic compound as well as preparation method and application thereof in OLED (organic light emitting diode) device

The invention discloses a fluorene-containing organic compound. The organic compound has the structure formula shown in the general formula (1). The compound has higher glass transition temperature and molecular heat stability, proper HOMO and LUMO energy levels and higher Eg, the photoelectric property of an OLED (organic light emitting diode) device can be effectively improved and the service life of the OLED device can be effectively prolonged through structure optimization of the device.

PURINE DERIVATIVES USEFUL AS HSP90 INHIBITORS

The present application provides substituted purine derivatives and related compounds of the formulas shown. These com ounds are useful as inhibitors of HSP90, and hence in the treatment of related diseases. (Formulae) Z1-Z3, Xa-Xc, X2, X4, Y and R are as defined in the specification.