ChemicalBook--->CAS DataBase List--->2351-50-0

2351-50-0

2351-50-0 Structure

2351-50-0 Structure
IdentificationBack Directory
[Name]

4-IODOSTYRENE
[CAS]

2351-50-0
[Synonyms]

4-IODOSTYRENE)
1-Ethenyl-4-iodobenzene
Benzene, 1-ethenyl-4-iodo-
KWHSBYQFELZKKS-UHFFFAOYSA-N
1-Ethenyl-4-iodobenzene, 1-Iodo-4-vinylbenzene
[Molecular Formula]

C8H7I
[MDL Number]

MFCD00045321
[MOL File]

2351-50-0.mol
[Molecular Weight]

230.05
Chemical PropertiesBack Directory
[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
[InChI]

InChI=1S/C8H7I/c1-2-7-3-5-8(9)6-4-7/h2-6H,1H2
[InChIKey]

KWHSBYQFELZKKS-UHFFFAOYSA-N
[SMILES]

C1(C=C)=CC=C(I)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2903998090
Spectrum DetailBack Directory
[Spectrum Detail]

4-IODOSTYRENE(2351-50-0)1HNMR
4-IODOSTYRENE(2351-50-0)FT-IR
Hazard InformationBack Directory
[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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