386267-31-8

Basic information

• Product Name: Ethyl 3-bromo-4-iodobenzoate
• Synonyms: Ethyl 3-bromo-4-iodobenzoate
• CAS NO: 386267-31-8
• Molecular Formula: C9H8BrIO2
• Molecular Weight: 354.96709
• Product Categories: Acids & Esters;Bromine Compounds;Iodine Compounds
• Mol File: 386267-31-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 341.4±27.0 °C(Predicted)
• Appearance: /
• Density: 1.949±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: Ethyl 3-bromo-4-iodobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 3-bromo-4-iodobenzoate(386267-31-8)
• EPA Substance Registry System: Ethyl 3-bromo-4-iodobenzoate(386267-31-8)

Safety Data

• Hazardous Substances Data: 386267-31-8(Hazardous Substances Data)

Usage

General Description

Ethyl 3-bromo-4-iodobenzoate is a chemical compound that belongs to the class of esters. It is primarily used in organic synthesis and pharmaceutical research. Ethyl 3-bromo-4-iodobenzoate is often utilized as an intermediate in the production of various pharmaceuticals and agrochemicals. Ethyl 3-bromo-4-iodobenzoate is known for its ability to react with a variety of reagents to form new compounds, making it a versatile building block in organic chemistry. It has also been studied for its potential anti-inflammatory and analgesic properties, making it a compound of interest in drug discovery and development. Additionally, it is important to handle this chemical with proper care and adhere to safety guidelines, as it may pose potential health and environmental hazards.

Upstream product

• 7149-03-3 ethyl 3-bromo-4-aminobenzoate 
• 94-09-7 p-aminoethylbenzoate 

Relevant articles and documents

Flexible, Linear Chains Act as Baffles To Inhibit the Intramolecular Rotation of Molecular Turnstiles

In artificial molecular devices, flexible, linear chains typically exhibit very weak capability in inhibiting molecular motion. Herein, we describe the dynamic properties of a series of molecular turnstiles consisting of a rigid frame and a phenyl rotator flanked with linear alkoxymethyl substituents. The long, flexible substituents act as elastic baffles to inhibit the rotations of the rotator at medium to fast speeds on the NMR time scale. When the rotator moves slowly, the substituents become more relaxed, thus obtaining an opportunity to completely thread through the cavity of the turnstiles. These findings reveal a basic but missing correlation between steric hindrance and speed of motion for flexible, linear chains in dynamic molecular devices, thus opening up a new direction toward molecular machines with more elaborate dynamic functions.

Synthesis of pyrene containing building blocks for dendrimer synthesis

Efficient syntheses of the novel, pyrene containing branched building blocks 10, 13, 22, 25 and of a pyrene based core molecule 16 for the construction of dendrimers are reported. The main tool is a Suzuki cross-coupling. The functional groups for further growth are amines and carboxylic acids, which were used in an orthogonally protected fashion. It was proven that the building blocks could be assembled to a low generation dendrimer 17.