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35371-03-0

35371-03-0 Structure

35371-03-0 Structure
IdentificationMore
[Name]

4-IODOTHIOANISOLE
[CAS]

35371-03-0
[Synonyms]

4-IODOTHIOANISOLE
4-Iodothiaanisole
(4-iodophenyl)(methyl)sulfane
1-(Methylthio)-4-iodobenzene
1-Iodo-4-(methylthio)benzene
Methyl p-iodophenyl sulfide
Methyl(4-iodophenyl) sulfide
p-Iodothioanisole
[Molecular Formula]

C7H7IS
[MDL Number]

MFCD00041454
[Molecular Weight]

250.1
[MOL File]

35371-03-0.mol
Chemical PropertiesBack Directory
[Melting point ]

40 °C
[Boiling point ]

262.6±23.0 °C(Predicted)
[density ]

1.78±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[Appearance]

Light brown to brown Solid
[CAS DataBase Reference]

35371-03-0(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[HS Code ]

29309090
Hazard InformationBack Directory
[Chemical Properties]

In solution, 4-Iodothioanisole shows a yellowish color due to intramolecular excitation of the cyclopentene system, while in the solid state it is orange because of free rotation around the carbon-iodine bond.It reacts with electrophiles to form carbon-iodine bonds and can be used to make cross-coupling reactions.
[Uses]

4-Iodothioanisole is a synthetic molecule that is used in organic chemistry as a reagent for the formation of carbon-carbon bonds. It also enhances the fluorescence of some molecules and has been used in supramolecular chemistry.
[Synthesis]

4-(Methylthio)phenylboronic acid

98546-51-1

4-IODOTHIOANISOLE

35371-03-0

General procedure for the synthesis of 4-iodoanisole from 4-methylthiophenylboronic acid: KX (X = I, Br) (0.2 mmol), 4-methylthiophenylboronic acid (0.3 mmol), CuBr2 (4.5 mg, 10 mol%), 1,10-phenanthroline (7.2 mg, 20 mol%), and DMF ( 2 mL). The reaction mixture was stirred at 80 °C or 130 °C for the reaction. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the residue was purified by rapid column chromatography on silica gel to afford the target product 4-iodoanisole.

[References]

[1] Tetrahedron Letters, 2011, vol. 52, # 16, p. 1993 - 1995
[2] Tetrahedron Letters, 2015, vol. 56, # 9, p. 1122 - 1123
[3] RSC Advances, 2015, vol. 5, # 103, p. 84910 - 84919
Spectrum DetailBack Directory
[Spectrum Detail]

4-IODOTHIOANISOLE(35371-03-0)1HNMR
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