- 4-Iodobenzonitrile
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- $100.00 / 1KG
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2025-09-25
- CAS:3058-39-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- 4-Iodobenzonitrile
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- $1.00 / 1kg
-
2019-07-06
- CAS:3058-39-7
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 500kg
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| | 4-Iodobenzonitrile Basic information |
| | 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 | | InChI | InChI=1S/C7H4IN/c8-7-3-1-6(5-9)2-4-7/h1-4H | | InChIKey | XOKDXPVXJWTSRM-UHFFFAOYSA-N | | SMILES | C(#N)C1=CC=C(I)C=C1 | | CAS DataBase Reference | 3058-39-7(CAS DataBase Reference) | | NIST Chemistry Reference | Benzonitrile, 4-iodo-(3058-39-7) | | EPA Substance Registry System | Benzonitrile, 4-iodo- (3058-39-7) |
| 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 | TSCA listed | | HazardClass | 6.1 | | PackingGroup | III | | HS Code | 29269090 | | Storage Class | 11 - Combustible Solids |
| | 4-Iodobenzonitrile Usage And Synthesis |
| Chemical Properties | light yellow crystal powder | | Uses | suzuki reaction | | Uses | 4-Iodobenzonitrile is used in organic synthesis. It is used as catalytic agent, petrochemical additive. | | Uses | 4-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 process
2-(4-cyanophenyl)tellurophene obtained via Stille coupling with tellurophene
2,5-bis(4-cyanophenyl)tellurophene obtained via Stille coupling with 2,5-bis(trimethylstannyl)tellurophene
ethyl-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: 10.1080/00397918808078799
Tetrahedron Letters, 35, p. 5539, 1994 DOI: 10.1016/S0040-4039(00)77241-8 | | Synthesis | A mixed solvent consisting of 0.2 mmol p-iodophenylacetic acid, 0.33 mmol cuprous bromide, 1.0 mL of acetonitrile and DMAc was added to the reactor (volume ratio [2:1]). The reaction was heated to 120 ??C under oxygen with continuous stirring for 34 h. The reaction was stopped, cooled to room temperature, washed by adding saturated ammonium chloride solution, extracted with ethyl acetate, dried, and the solvent was removed by distillation under reduced pressure, and the crude product was separated by column chromatography to give 4-iodocyanobenzene in 61% yield.
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| | 4-Iodobenzonitrile Preparation Products And Raw materials |
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