ChemicalBook Product Catalog Chemical Reagents Organic reagents Cyanide / nitrile 2-Iodobenzonitrile

2-Iodobenzonitrile

2-Iodobenzonitrile Basic information
Product Name:2-Iodobenzonitrile
Synonyms:1-CYANO-2-IODOBENZENE;O-IODOBENZONITRILE;2-IODOBENZONITRILE;2-iodobenzontirlle;2-Iodobenzonitrile,99%;2-lodobenzonitrile;Nitrile o-iodobenzene;2-Iodobenzonitrile 97%
CAS:4387-36-4
MF:C7H4IN
MW:229.02
EINECS:
Product Categories:Building Blocks;C6 to C7;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Aromatic Nitriles;Nitrile;Iodine Compounds;Nitriles;C6 to C7;Cyanides/Nitriles;Nitrogen Compounds
Mol File:4387-36-4.mol
2-Iodobenzonitrile Structure
2-Iodobenzonitrile Chemical Properties
Melting point 52-54°C
Boiling point 147 °C / 15mmHg
density 1.91±0.1 g/cm3(Predicted)
Fp 110 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form Solid
color Yellow
CAS DataBase Reference4387-36-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38-36-22
Safety Statements 26-36/37/39
RIDADR 3439
WGK Germany 3
Hazard Note Harmful
HazardClass IRRITANT-HARMFUL
PackingGroup III
HS Code 29269090
MSDS Information
2-Iodobenzonitrile Usage And Synthesis
Chemical PropertiesYellow solid
Uses2-Iodobenzonitrile is a nitrile compound. Nitrile compounds are one of the most important organic synthesis intermediates in organic synthetic chemistry and are widely used in pesticides, pharmaceuticals, dyes and other fine chemicals. Moreover, because o-iodobenzonitrile compounds contain both cyano and aryl carbon-iodide bonds, and both of them are in the adjacent position of benzene ring, 2-iodobenzonitrile can have excellent reactivity when used as intermediates.
Usessuzuki reaction
2-Iodobenzonitrile Preparation Products And Raw materials
Preparation Products2-ethylquinazolin-4-ol-->2-IODOBENZAMIDE-->1-Boc-3-aminoindazole-->2-(3-Methyl-1,2,4-oxadiazol-5-yl)benzoic acid-->2-[(TRIMETHYLSILYL)ETHYNYL]BENZONITRILE-->2,2'-DITHIOBIS(BENZONITRILE)-->2-(4-Chlorophenyl)benzonitrile-->4-BROMO-2'-CYANOBIPHENYL
2-IODO-3-METHYLBENZONITRILE 3-BROMO-5-IODOBENZONITRILE 2-Chloro-6-iodobenzonitrile (Diacetoxyiodo)benzene 3-FLUORO-5-IODOBENZONITRILE,5-FLUORO-3-IODOBENZONITRILE 3-CYANO-2-IODOBENZOTRIFLUORIDE 4-CHLORO-2-IODOBENZONITRILE 2,4-DICYANO-3-IODO-5-PHENYLBENZOTRIFLUORIDE 4-AMINO-3-IODOBENZONITRILE 2-IODO-6-(TRIFLUOROMETHYL)BENZONITRILE 2-Amino-5-bromo-6-fluoro-3-iodobenzonitrile 2-Fluoro-4-iodobenzonitrile 98%,2-Fluoro-4-iodobenzonitrile98%,2-FLUORO-4-IODOBENZONITRILE 5-FLUORO-2-IODOBENZONITRILE 5-CHLORO-2-IODOBENZONITRILE 5-Bromo-3-chloro-2-iodobenzonitrile 2,5-DIIODOBENZONITRILE Ioxynil 2-BROMO-5-IODOBENZONITRILE
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