4-Iodobenzonitrile

4-Iodobenzonitrile
  • CAS No.:3058-39-7
Other grades of this product :
4-Iodobenzonitrile Basic information
Product Name:4-Iodobenzonitrile
Synonyms:4-Iodobenzonitrile, 99% 25GR;4-Iodobenzonitrile ,98%;4-lodobenzonitrile;Benzonitrile of iodine;On iodobenzene nitrile;Benzonitrile, 4-iodo-;On ioxynil;4-iodo-benzonitril
CAS:3058-39-7
MF:C7H4IN
MW:229.02
EINECS:
Product Categories:Building Blocks;C6 to C7;API intermediates;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Aromatic Nitriles;Iodine Compounds;Nitriles;C6 to C7;Cyanides/Nitriles;Nitrogen Compounds
Mol File:3058-39-7.mol
4-Iodobenzonitrile Chemical Properties
Melting point 124-128 °C(lit.)
Boiling point 271.6±23.0 °C(Predicted)
density 1.9241 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Powder or Chunks
color Light yellow-brown
Water Solubility Insoluble in water.
Sensitive Light Sensitive
CAS DataBase Reference3058-39-7(CAS DataBase Reference)
NIST Chemistry ReferenceBenzonitrile, 4-iodo-(3058-39-7)
EPA Substance Registry SystemBenzonitrile, 4-iodo- (3058-39-7)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 36/37/38-20/21/22
Safety Statements 22-24/25-36/37/39-26
RIDADR 3439
WGK Germany 3
Hazard Note Irritant
TSCA Yes
HazardClass 6.1
PackingGroup III
HS Code 29269090
MSDS Information
ProviderLanguage
p-Iodobenzonitrile English
ACROS English
SigmaAldrich English
ALFA English
4-Iodobenzonitrile Usage And Synthesis
Chemical Propertieslight yellow crystal powder
Usessuzuki reaction
Uses4-Iodobenzonitrile is used in organic synthesis. It is used as catalytic agent, petrochemical additive.
Uses4-Iodobenzonitrile may be used in the synthesis of the following:ethyl-4′-cyano-4-nitro[1,1′-biphenyl]-2-carboxylate via a multi-step reaction process2-(4-cyanophenyl)tellurophene obtained via Stille coupling with tellurophene2,5-bis(4-cyanophenyl)tellurophene obtained via Stille coupling with 2,5-bis(trimethylstannyl)telluropheneethyl-4′-cyano-6-{[(E)-phenylmethylidene]amino}[1,1′-biphenyl]-3-carboxylate via a multi-step reaction process
Synthesis Reference(s)Synthetic Communications, 18, p. 1327, 1988 DOI: 10.1080/00397918808078799Tetrahedron Letters, 35, p. 5539, 1994 DOI: 10.1016/S0040-4039(00)77241-8

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