4-Bromobenzaldehyde CAS 1122-91-4 Purity >99.0% (GC) Factory
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Chemical Name | 4-Bromobenzaldehyde |
Synonyms | p-Bromobenzaldehyde; 4-BBA |
CAS Number | 1122-91-4 |
CAT Number | RF-PI336 |
Stock Status | In Stock, Production Scale Up to Tons |
Molecular Formula | C7H5BrO |
Molecular Weight | 185.02 |
Melting Point | 55.0~58.0℃(lit.) |
Boiling Point | 66.0~68.0℃ at 2 mmHg |
Flash Point | 108°(226°F) |
Density | 1.85g/cm3 |
Sensitive | Air Sensitive |
Solubility | Insoluble in Water; Soluble in Ether, Alcohols |
Hazard Note | Irritant / Harmful / Air Sensitive |
Packing Group | III |
Storage Conditions | Room Temperature |
Brand | Ruifu Chemical |
Item | Specifications |
Appearance | White or Pale-Yellow Crystal |
Purity / Analysis Method | >99.0% (GC) |
4-Bromobenzoic Aicd | <0.70% (GC) |
Other Unknown Impurities | <0.30% (GC) |
Total Impurities | <1.00% |
Moisture (K.F) | <0.20% |
Test Standard | Enterprise Standard |
Usage | Organic & Pharmaceutical Synthesis Intermediate |
Package: Bottle, Aluminum foil bag, 25kg/Cardboard Drum, or according to customer's requirement
Storage Condition: Preserve in tight, light-resistant containers, refrigerated storage
4-Bromobenzaldehyde (CAS 1122-91-4) is a chemical compound that belongs to the group of aromatic compounds. 4-Bromobenzaldehyde is widely utilized as an intermediate for the preparation of agrochemicals, pharmaceuticals and other organic compounds. 4-Bromobenzaldehyde is part of a group of benzaldehydes that have in vivo antibacterial activity against Mycobacterium tuburculosis. It's also used as a reagent in the synthesis of 4-Bromobenzaldehyde semicarbazone, a trial compound of a novel class of anticonvulsants. 4-Bromobenzaldehyde is used as a precursor and reacts with sulfamethoxazole to prepare Schiffs 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.