4-IODOSTYRENE

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CAS:2351-50-0
Purity:0.99 Package:5KG;1KG
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CAS:2351-50-0
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CAS:2351-50-0
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CAS:2351-50-0
Purity:97% (stabilized with TBC) Package:5g, 250mg, 100mg, 1g
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Products Intro: Product Name:4-Iodostyrene
CAS:2351-50-0
Purity:99 Package:5KG;1KG

4-IODOSTYRENE manufacturers

  • 4-Iodostyrene
  • 4-Iodostyrene pictures
  • $0.00 / 1kg
  • 2025-06-04
  • CAS:2351-50-0
  • Min. Order: 1kg
  • Purity: 98%+
  • Supply Ability: 100000kg per Month
4-IODOSTYRENE Basic information
Product Name:4-IODOSTYRENE
Synonyms:4-IODOSTYRENE);Benzene, 1-ethenyl-4-iodo-;1-Ethenyl-4-iodobenzene, 1-Iodo-4-vinylbenzene;KWHSBYQFELZKKS-UHFFFAOYSA-N;1-Ethenyl-4-iodobenzene;DK686;DKFELEX0173;4-Iodostyrene,98% (stabilized with TBC)
CAS:2351-50-0
MF:C8H7I
MW:230.05
EINECS:
Product Categories:
Mol File:2351-50-0.mol
4-IODOSTYRENE Structure
4-IODOSTYRENE Chemical Properties
Melting point 44-44.5 °C
Boiling point 91-93 °C(Press: 6 Torr)
density 1.673±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form crystalline solid
color Off-white
InChIInChI=1S/C8H7I/c1-2-7-3-5-8(9)6-4-7/h2-6H,1H2
InChIKeyKWHSBYQFELZKKS-UHFFFAOYSA-N
SMILESC1(C=C)=CC=C(I)C=C1
Safety Information
HS Code 2903998090
MSDS Information
4-IODOSTYRENE Usage And Synthesis
Synthesis
Tetravinylsilane

1112-55-6

1,4-Diiodobenzene

624-38-4

P-DIVINYLBENZENE  85

105-06-6

4-IODOSTYRENE

2351-50-0

General procedure for the synthesis of p-dienylbenzene and 4-iodostyrene from tetravinylsilane and 1,4-diiodobenzene: 1,4-diiodobenzene (0.25 mmol), tetravinylsilane (0.15 mmol), potassium fluoride (1.2 mmol), and loaded palladium nanoparticle catalysts (Pd to substrate molar ratio of 1%) were suspended in N,N-dimethylformamide (1 mL). Subsequently, the reaction flask was evacuated and replaced with argon, and this evacuation-argon replacement cycle was repeated three times (operating pressure of 2 bar). The reaction mixture was stirred at 130°C for 3 h, during which the reaction progress was monitored by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). During this process, all the initial intermediates 3i'-j' formed by single iodide substitution were further reacted to maximize the yield of the target products 3i-j.

References[1] Journal of Catalysis, 2013, vol. 302, p. 49 - 57
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