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5-Iodo-m-xylene, 97%

CAS: 22445-41-6 | C8H9I | 232.06 g/mol

$96.93 - $324.82

Chemical Identifiers

CAS 22445-41-6
Molecular Formula C8H9I
Molecular Weight (g/mol) 232.06
MDL Number MFCD00060659
InChI Key ZLMKEENUYIUKKC-UHFFFAOYSA-N
Synonym 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, #
PubChem CID 140924
IUPAC Name 1-iodo-3,5-dimethylbenzene
SMILES CC1=CC(I)=CC(C)=C1
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Description

Description

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.
Specifications

Chemical Identifiers

22445-41-6
232.06
ZLMKEENUYIUKKC-UHFFFAOYSA-N
140924
CC1=CC(I)=CC(C)=C1
C8H9I
MFCD00060659
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, #
1-iodo-3,5-dimethylbenzene

Specifications

22445-41-6
229°C
1.595
MFCD00060659
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, #
ZLMKEENUYIUKKC-UHFFFAOYSA-N
1-iodo-3,5-dimethylbenzene
140924
98%
1.61
10 g
C8H9I
2039353
Sparingly soluble (0.014g/L) (25°C),Calc.
CC1=CC(I)=CC(C)=C1
232.06
232.07
5-Iodo-m-xylene
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

EINECSNumber : 000-000-0

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only