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5-Iodo-m-xylene, 97%, Thermo Scientific Chemicals

Catalog Number p-7024159
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Quantity:
10 g
50 g
This item is not returnable. View return policy
22445-41-6
C8H9I
232.06
MFCD00060659
ZLMKEENUYIUKKC-UHFFFAOYSA-N
5-iodo-m-xylene, 1,3-dimethyl-5-iodobenzene, benzene, 1-iodo-3,5-dimethyl, 3,5-dimethyliodobenzene, pubchem3872, acmc-1ccdf, 3,5-dimethyl-1-iodobenzene, ksc422q9l, 1-iodo-3,5-dimethylbenzene, #
140924
1-iodo-3,5-dimethylbenzene
CC1=CC(I)=CC(C)=C1
This item is not returnable. View return policy
22445-41-6
C8H9I
232.06
MFCD00060659
ZLMKEENUYIUKKC-UHFFFAOYSA-N
5-iodo-m-xylene, 1,3-dimethyl-5-iodobenzene, benzene, 1-iodo-3,5-dimethyl, 3,5-dimethyliodobenzene, pubchem3872, acmc-1ccdf, 3,5-dimethyl-1-iodobenzene, ksc422q9l, 1-iodo-3,5-dimethylbenzene, #
140924
1-iodo-3,5-dimethylbenzene
CC1=CC(I)=CC(C)=C1

1-Iodo-3,5-dimethylbenzene (5-iodo-m-xylene) is suitable for use in the synthesis of N-(3,5-xylyl)-N-ethyl aniline, an aryl amine, It is also used in the following studies; α-Arylation of ketones, Copper-catalyzed N-arylation of imidazoles, Cyanation of 5-iodo-m-xylene to form 3,5-dimethylbenzonitrile, synthesis of 1,3-Dimethyl-5-phenoxybenzene by nano-CuFe2O4 catalyzed C-O cross-coupling with phenol, CuBr-catalyzed amination of 1-iodo-3,5-dimethylbenzene to form N-Allyl-3,5-dimethylbenzenamine, copper-catalyzed C-S bond-formation between 5-iodo-m-xylene and thiophenol. It is also employed as a starting material in the synthesis of biphenyl-3,3’,5,5’-tetracarboxylic acid, radical bromination of 5-iodo-m-xylene by N-bromosuccinimide to form 1,3-bis(bromomethyl)-5-iodobenzene.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1-Iodo-3,5-dimethylbenzene (5-iodo-m-xylene) is suitable for use in the synthesis of N-(3,5-xylyl)-N-ethyl aniline, an aryl amine, It is also used in the following studies; α-Arylation of ketones, Copper-catalyzed N-arylation of imidazoles, Cyanation of 5-iodo-m-xylene to form 3,5-dimethylbenzonitrile, synthesis of 1,3-Dimethyl-5-phenoxybenzene by nano-CuFe2O4 catalyzed C-O cross-coupling with phenol, CuBr-catalyzed amination of 1-iodo-3,5-dimethylbenzene to form N-Allyl-3,5-dimethylbenzenamine, copper-catalyzed C-S bond-formation between 5-iodo-m-xylene and thiophenol. It is also employed as a starting material in the synthesis of biphenyl-3,3’,5,5’-tetracarboxylic acid, radical bromination of 5-iodo-m-xylene by N-bromosuccinimide to form 1,3-bis(bromomethyl)-5-iodobenzene.

Solubility
Sparingly soluble (0.014 g/L) (25°C), Calc.

Notes
Light Sensitive. Store away from oxidizing agents and light. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
TRUSTED_SUSTAINABILITY
Density 1.61
Boiling Point 229°C
Quantity 10 g
Refractive Index 1.595
Beilstein 2039353
Solubility Information Sparingly soluble (0.014g/L) (25°C),Calc.
Formula Weight 232.07
Percent Purity 98%
Chemical Name or Material 5-Iodo-m-xylene

RUO – Research Use Only

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