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4-Bromobenzaldehyde, 98+%
CAS: 1122-91-4 | C7H5BrO | 185.02 g/mol
$155.70 - $1676.90
Chemical Identifiers
| CAS | 1122-91-4 |
|---|---|
| Molecular Formula | C7H5BrO |
| Molecular Weight (g/mol) | 185.02 |
| MDL Number | MFCD00003377 |
| InChI Key | ZRYZBQLXDKPBDU-UHFFFAOYSA-N |
| Synonym | p-bromobenzaldehyde, benzaldehyde, 4-bromo, benzaldehyde, p-bromo, 4-bromo-benzaldehyde, 4-bromo benzaldehyde, 4-bromobenzylaldehyde, p-bromo benzaldehyde, unii-4l8vm24f65, 4-brombenzaldehyde, 4-brombenzaldehyd |
| PubChem CID | 70741 |
| IUPAC Name | 4-bromobenzaldehyde |
| SMILES | C1=CC(=CC=C1C=O)Br |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1423714
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Thermo Scientific Chemicals
A1423714 |
25 g |
Each for $155.70
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AAA1423722
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Thermo Scientific Chemicals
A1423722 |
100 g |
Each for $431.30
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AAA1423736
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Thermo Scientific Chemicals
A1423736 |
500 g |
Each for $1,676.90
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Description
4-Bromobenzaldehyde is widely utilized as an intermediate for the preparation of agrochemicals, pharmaceuticals and other organic compounds. It is used as a precursor and reacts with sulfamethoxazole to prepare Schiffâs base, 4-[(4-Bromo-benzylidene)-amino]-N-(5-methyl-isoxazol-3-yl)-benzene sulfonamide, which can be used for the photo stability of polyvinyl chloride (PVC). It plays an important role in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes. It is employed in a cross-coupling study with potassium vinyltrifluoroborate.
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.
Applications4-Bromobenzaldehyde is widely utilized as an intermediate for the preparation of agrochemicals, pharmaceuticals and other organic compounds. It is used as a precursor and reacts with sulfamethoxazole to prepare Schiffâs base, 4-[(4-Bromo-benzylidene)-amino]-N-(5-methyl-isoxazol-3-yl)-benzene sulfonamide, which can be used for the photo stability of polyvinyl chloride (PVC). It plays an important role in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes. It is employed in a cross-coupling study with potassium vinyltrifluoroborate.
Solubility
Soluble in ethanol and benzene. Insoluble in water.
Notes
Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong bases, strong oxidizing agents and strong reducing agents.
Chemical Identifiers
| 1122-91-4 | |
| 185.02 | |
| ZRYZBQLXDKPBDU-UHFFFAOYSA-N | |
| 70741 | |
| C1=CC(=CC=C1C=O)Br |
| C7H5BrO | |
| MFCD00003377 | |
| p-bromobenzaldehyde, benzaldehyde, 4-bromo, benzaldehyde, p-bromo, 4-bromo-benzaldehyde, 4-bromo benzaldehyde, 4-bromobenzylaldehyde, p-bromo benzaldehyde, unii-4l8vm24f65, 4-brombenzaldehyde, 4-brombenzaldehyd | |
| 4-bromobenzaldehyde |
Specifications
| 1122-91-4 | |
| 66°C to 68°C (2 mmHg) | |
| Characteristic | |
| MFCD00003377 | |
| 507100 | |
| p-bromobenzaldehyde, benzaldehyde, 4-bromo, benzaldehyde, p-bromo, 4-bromo-benzaldehyde, 4-bromo benzaldehyde, 4-bromobenzylaldehyde, p-bromo benzaldehyde, unii-4l8vm24f65, 4-brombenzaldehyde, 4-brombenzaldehyd | |
| ZRYZBQLXDKPBDU-UHFFFAOYSA-N | |
| 4-bromobenzaldehyde | |
| 70741 | |
| ≥98% |
| 55°C to 58°C | |
| 108°C (226°F) | |
| C7H5BrO | |
| 25 g | |
| Air Sensitive | |
| Soluble in ethanol and benzene. Insoluble in water. | |
| C1=CC(=CC=C1C=O)Br | |
| 185.02 | |
| 185.03 | |
| 4-Bromobenzaldehyde |
Safety and Handling
GHS H Statement
H302-H315-H319-H335
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P270-P271-P280-P285-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P342+P311-P362-P501c
H302-H315-H319-H334-H335
EINECSNumber : 214-365-0
RTECSNumber : CU4810000
TSCA : Yes
Recommended Storage : Ambient temperatures; Store under Nitrogen
RUO – Research Use Only