99847-42-4

Basic information

• Product Name: 4-CHLORO-4'-IODOBENZOPHENONE
• Synonyms: 4-CHLORO-4'-IODOBENZOPHENONE;(4-CHLOROPHENYL)(4-IODOPHENYL)METHANONE
• CAS NO: 99847-42-4
• Molecular Formula: C₁₃H₈ClIO
• Molecular Weight: 342.56
• Mol File: 99847-42-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 401.5°C at 760 mmHg
• Flash Point: 196.6°C
• Appearance: /
• Density: 1.699g/cm³
• Vapor Pressure: 1.17E-06mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: 4-CHLORO-4'-IODOBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-4'-IODOBENZOPHENONE(99847-42-4)
• EPA Substance Registry System: 4-CHLORO-4'-IODOBENZOPHENONE(99847-42-4)

Safety Data

• Hazardous Substances Data: 99847-42-4(Hazardous Substances Data)

Usage

Description

4-CHLORO-4'-IODOBENZOPHENONE is a chemical compound belonging to the benzophenone class, characterized by a benzophenone core with a chloro and iodo substituent at the 4 and 4' positions, respectively. It is a white to slightly yellow crystalline powder with a molecular weight of 302.12 g/mol.

Uses

Used in Pharmaceutical Industry:
4-CHLORO-4'-IODOBENZOPHENONE is used as a building block in the synthesis of pharmaceuticals for its versatile chemical structure, which can be further modified to create various medicinal compounds.
Used in Agrochemical Industry:
4-CHLORO-4'-IODOBENZOPHENONE is used as a building block in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Organic Compounds Synthesis:
4-CHLORO-4'-IODOBENZOPHENONE is used as a building block for the synthesis of other organic compounds, owing to its unique structure that allows for a wide range of chemical reactions and modifications.

InChI:InChI=1/C13H8ClIO/c14-11-5-1-9(2-6-11)13(16)10-3-7-12(15)8-4-10/h1-8H

Upstream product

• 106-39-8 bromochlorobenzene 
• 24167-53-1 4-iodo-N,N-dimethylbenzamide 
• 51934-41-9 4-iodobenzoic acid ethyl ester 
• 108-90-7 chlorobenzene 
• 1711-02-0 4-iodobenzoic acid chloride 

Downstream Products

• 917899-60-6 3-(4-chloro-phenyl)-3-hydroxy-3-(4-iodo-phenyl)propionitrile 
• 857532-14-0 2-[2-(4-chloro-phenyl)-2-hydroxy-2-(4-iodo-phenyl)-ethyl]-isoindole-1,3-dione 
• 857532-01-5 1-(4-chloro-phenyl)-2-(2-hydroxy-ethylamino)-1-(4-iodo-phenyl)-ethanol 
• 857532-02-6 2-(4-chloro-phenyl)-2-(4-iodo-phenyl)-morpholine 
• 1056901-66-6 (RS)-2-ammonio-1-(4-chlorophenyl)-1-(4-iodophenyl)ethanol toluene-4-sulphonate 
• 1056901-64-4 2-(4-chloro-phenyl)-2-hydroxy-2-[4-(1H-pyrazol-4-yl)-phenyl]-ethyl-carbamic acid tert-butyl ester 
• 1056901-63-3 [2-(4-chloro-phenyl)-2-hydroxy-2-(4-iodo-phenyl)ethyl]-carbamic acid tert-butyl ester 
• 1056901-65-5 (RS)-2-azido-1-(4-chlorophenyl)-1-(4-iodophenyl)ethanol 
• 917899-14-0 2-amino-1-(4-chloro-phenyl)-1-(4-iodo-phenyl)-ethanol 
• 857532-13-9 2-amino-1-(4-chloro-phenyl)-1-[4-(1H-pyrazol-4-yl)-phenyl]-ethanol 
• 857532-00-4 (RS)-2-(4-chloro-phenyl)-2-(4-iodo-phenyl)-oxirane 
• 172219-25-9 ethyl 1-<2-<(4-chlorophenyl)(4-iodophenyl)>methoxyethyl>piperidine-4-carboxylate 
• 172219-26-0 <2-<(4-chlorophenyl)(4-iodophenyl)>methoxyethyl>-1-piperidine-3-carboxylic acid 
• 172219-24-8 1-chloro-4-(chloro(4-iodophenyl)methyl)benzene 

Relevant articles and documents

Continuous Flow Acylation of (Hetero)aryllithiums with Polyfunctional N,N-Dimethylamides and Tetramethylurea in Toluene

The continuous flow reaction of various aryl or heteroaryl bromides in toluene in the presence of THF (1.0 equiv) with sec-BuLi (1.1 equiv) provided at 25 °C within 40 sec the corresponding aryllithiums which were acylated with various functionalized N,N-