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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 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1841309
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Thermo Scientific Chemicals
A1841309 |
10 g |
Each for $96.93
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AAA1841318
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Thermo Scientific Chemicals
A1841318 |
50 g |
Each for $324.82
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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-3,3â,5,5â-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.
Applications1-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-3,3â,5,5â-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.
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 |
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
RUO – Research Use Only