57830-60-1

Basic information

• Product Name: 1,3-Diiodo-5-nitrobenzene
• Synonyms: 1,3-Diiodo-5-nitrobenzene;Benzene, 1,3-diiodo-5-nitro-;JIVYEUNBDFYQRD-UHFFFAOYSA-N
• CAS NO: 57830-60-1
• Molecular Formula: C₆H₃I₂NO₂
• Molecular Weight: 374.90246
• Mol File: 57830-60-1.mol
• Article Data: 22

Chemical Properties

• Melting Point: 104.5 °C
• Boiling Point: 365.7±22.0 °C(Predicted)
• Appearance: /
• Density: 2.578±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,3-Diiodo-5-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Diiodo-5-nitrobenzene(57830-60-1)
• EPA Substance Registry System: 1,3-Diiodo-5-nitrobenzene(57830-60-1)

Safety Data

• Hazardous Substances Data: 57830-60-1(Hazardous Substances Data)

Usage

General Description

1,3-Diiodo-5-nitrobenzene is a chemical compound with the molecular formula C6H3I2NO2. It is a yellow crystalline solid that is primarily used as a building block in the synthesis of various organic compounds. 1,3-Diiodo-5-nitrobenzene is a nitrobenzene derivative, meaning it contains a nitro group (NO2) attached to a benzene ring. The presence of two iodine atoms in the 1 and 3 positions of the benzene ring gives this compound its unique properties and reactivity. 1,3-Diiodo-5-nitrobenzene is often used in organic and pharmaceutical synthesis, as well as in the creation of dyes and pigments due to its colorful and reactive nature. 1,3-Diiodo-5-nitrobenzene should be handled with care as it may pose health hazards if not handled properly.

Upstream product

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Downstream Products

• 306272-08-2 1,3-bis(trimethylsilylethynyl)-5-nitrobenzene 
• 1421030-00-3 4-phenyl-3-(3,5-bis(2,4,6-trimethylphenyl)phenyldiazenyl)pyridine 
• 1000289-42-8 1-benzoyl-3-(3,5-diiodophenyl)thiourea 
• 1000289-43-9 (3,5-diiodophenyl)thiourea 
• 954105-35-2 1-(3,5-diiodophenyl)-3,3-diethyltriaz-1-ene 
• 1312923-90-2 3-(2-(2-methylthiazol-4-yl)ethynyl)-5-nitroiodobenzene 
• 6286-37-9 acetic acid-(3,5-diiodo-anilide) 

Relevant articles and documents

Preparation and application of a D-A conjugated electrochromic flexible electrode with side chain carbazole active groups in supercapacitors

Electrochromic power storage devices (ESCs) integrate energy storage and electrochromic behaviour into a single full cell that can enable the visualization of the energy status by the naked eye. One challenge for achieving practical applications is the development of intelligent and portable all-organic electrochromic power storage devices. Donor-acceptor (D-A) polymers have been widely studied for their tunable electronic properties. However, studies of polymers with optoelectrochemical, electrochromic and electrochemical performance substituted with different carbazole groups have drawn little attention. Herein, we designed and synthesized four polymers with carbazole side chains. The polymer solutions can be simply processed into thin films. Meanwhile, they exhibit an obvious and reversible colour transition between red (uncharged state) and dark blue (charged state), with an optical contrast of 37.35% and a colouring efficiency of 241.40 cm2 C-1 at a wavelength of 661 nm. The electrochromic components of PI-2 and PI-3 were assembled and proved to be able to change colour in the bending state. Hence, the energy storage level of the ESCs is directly related to their colour and can be determined by the naked eye, which means that they can be incorporated with other energy cells to visually display their energy status. PI-3 was assembled into a flexible supercapacitor that lighted up a 1.5 V light-emitting diode. Finally, the results present significant potential of PI-3 electrodes for efficient energy storage and electrochromic properties with stable transmittance changes, demonstrating their potential as smart wearable energy storage devices. This work can provide a platform for developing smart and portable power storage devices with enhanced energy densities.

Reduction-rebridging strategy for the preparation of ADPN-based antibody-drug conjugates

The reduction-rebridging strategy is a powerful method for the preparation of stable and homogeneous antibody-drug conjugates (ADCs). In this communication, we describe the development of the arylene-dipropiolonitrile (ADPN) functional group for the rebri

3,5-diiodo benzenesulfonyl choride preparation technology

The invention discloses a 3,5-diiodo benzenesulfonyl choride preparation technology. The preparation technology comprises the following steps: taking paranitroaniline as a raw material, performing a substitution reaction to generate 2,6-diiodo-4-nitro aniline, performing diazotization and hydrolysis on 2,6-diiodo-4-nitro aniline and performing hydrolysis to generate 3,5-diodonitrobenzene, performing a reduction reaction on the 3,5-diodonitrobenzene to generate 3,5-diiodoaniline, performing diazotization and a sulfonylation reaction on the 3,5-diiodoaniline to obtain a target compound 3,5-diiodo benzenesulfonyl choride. The technology has the advantages of easily available raw materials, simple operation and post-treatment, and high yield, and is suitable for industrial production.