130723-54-5

Basic information

• Product Name: 3-IODOPHENYLACETONITRILE
• Synonyms: 3-IODOPHENYLACETONITRILE;3-IODOBENZYL CYANIDE;3-Iodobenzyl Cyanide 130723-54-5;2-(3-Iodophenyl)acetonitrile;m-Iodobenzyl cyanide;3-Iodophenylacetonitrile 90%
• CAS NO: 130723-54-5
• Molecular Formula: C₈H₆IN
• Molecular Weight: 243.04
• EINECS: -0
• Product Categories: C8 to C9;Cyanides/Nitriles;Nitrogen Compounds;Building Blocks;C8 to C9;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks
• Mol File: 130723-54-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 34-38 °C(lit.)
• Boiling Point: 138°C 12mm
• Flash Point: 138°C/12mm
• Appearance: /
• Density: 1.764g/cm³
• Vapor Pressure: 0.000674mmHg at 25°C
• Refractive Index: 1.624
• Storage Temp.: 2-8°C(protect from light)
• Solubility: soluble in Methanol
• Water Solubility: Insoluble in water
• Sensitive: Light Sensitive
• BRN: 7350695
• CAS DataBase Reference: 3-IODOPHENYLACETONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-IODOPHENYLACETONITRILE(130723-54-5)
• EPA Substance Registry System: 3-IODOPHENYLACETONITRILE(130723-54-5)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 20/21/22-36/37/38-21/22
• Safety Statements: 36/37
• RIDADR: 3439
• WGK Germany: 3
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 130723-54-5(Hazardous Substances Data)

Usage

Description

3-IODOPHENYLACETONITRILE, also known as 3-Iodophenylacetic acid nitrile, is an organic compound with the chemical formula C8H6I2N. It is a derivative of phenylacetic acid, featuring a nitrile group and an iodine atom attached to the benzene ring. 3-IODOPHENYLACETONITRILE is known for its unique chemical properties and is widely utilized in various industries due to its versatile applications.

Uses

Used in Agrochemical Industry:
3-IODOPHENYLACETONITRILE is used as an intermediate compound for the synthesis of various agrochemicals, such as pesticides and herbicides. Its presence in these products aids in enhancing their effectiveness in controlling pests and weeds, ultimately contributing to increased crop yields and improved agricultural productivity.
Used in Pharmaceutical Industry:
3-IODOPHENYLACETONITRILE is employed as a key intermediate in the development of pharmaceutical drugs. Its unique chemical structure allows it to be used in the synthesis of various therapeutic agents, including those targeting cancer, inflammation, and other medical conditions. The compound's versatility makes it a valuable asset in the ongoing search for novel and effective medications.
Used in Dyestuff Industry:
3-IODOPHENYLACETONITRILE is utilized as a crucial component in the production of dyes and pigments. Its chemical properties enable it to impart vibrant colors and enhanced stability to the final products, making it an essential ingredient in the creation of a wide range of dyes used in various applications, such as textiles, plastics, and printing inks.

InChI:InChI=1/C8H6IN/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6H,4H2

Upstream product

• 31938-07-5 (3-bromophenyl)acetonitrile 
• 151-50-8 potassium cyanide 
• 49617-83-6 m-Iodobenzyl bromide 
• 130723-53-4 3-(2-Cyanoprop-2-yl)phenyl iodide 

Downstream Products

• 30118-03-7 2-(3-Iodo-phenyl)-3-oxo-butyronitrile 
• 189278-01-1 (1S,3R,5R)-3-(3-Iodo-phenyl)-8-oxa-bicyclo[3.2.1]octane-3-carbonitrile 
• 189139-52-4 (1R,3S,5S)-3-(3-Iodo-phenyl)-8-oxa-bicyclo[3.2.1]octane-3-carbonitrile 
• 179421-14-8 4-cyano-4-(3-iodophenyl)-3,4,5,6-tetrahydro-2H-pyran 
• 278183-73-6 4-cyano-4-{3-[4-(2-methyl-1H-imidazol-1-yl)phenylthio]}phenyl-3,4,5,6-tetrahydro-2H-pyran 
• 179421-15-9 4-cyano-4-{3-[tri-(1-methylethyl)]silylthiophenyl}-3,4,5,6-tetrahydro-2H-pyran 
• 179420-17-8 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxamide 
• 179421-18-2 4-(3-Iodophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carbadehyde 
• 179420-40-7 4-[3-(4-[1,2,4]triazol-4-yl-phenylsulfanyl)-phenyl]-tetrahydro-pyran-4-carbonitrile 
• 179420-48-5 4-[3-[4(2-Methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carbaldehyde 
• 179421-20-6 [4-[3-[4-(2-Methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro2H-pyran-4yl]methanol 
• 179420-47-4 methyl 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate 
• 179420-42-9 4-{3-[4-(3,5-dimethyl-pyrazol-1-yl)-phenylsulfanyl]-phenyl}-tetrahydro-pyran-4-carbonitrile 
• 189277-92-7 (1S,3R,5R)-3-{3-[4-(2-Methyl-imidazol-1-yl)-phenylsulfanyl]-phenyl}-8-oxa-bicyclo[3.2.1]octane-3-carbonitrile 

Relevant articles and documents

Rapid and efficient copper-catalyzed finkelstein reaction of (hetero)aromatics under continuous-flow conditions

A general, rapid, and efficient method for the copper-catalyzed Finkelstein reaction of (hetero)aromatics has been developed using continuous flow to generate a variety of aryl iodides. The described method can tolerate a broad spectrum of functional groups, including N-H and O-H groups. Additionally, in lieu of isolation, the aryl iodide solutions were used in two distinct multistep continuous-flow processes (amidation and Mg-I exchange/nucleophilic addition) to demonstrate the flexibility of this method.

Organic compounds

Compounds of general formula (I) wherein the substituents are as defined in claim 1 are suitable for use as herbicides.