Aryl bromides
![Frontier Specialty Chemicals 1g, 4-Bromo-3-trifluoromethyl-1H-pyrazole, 98%, [19968-17-3], B10918 214.971 C4H2BrF3N2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Frontier Specialty Chemicals 1g, 4-Bromo-3-trifluoromethyl-1H-pyrazole, 98%, [19968-17-3], B10918 214.971 C4H2BrF3N2
Compound: 4-Bromo-3-trifluoromethyl-1H-pyrazole
CAS#: 19968-17-3
MDL#: not listed
Background: A brominated, trifluoromethylated pyrazole used as a building block in pharmaceutical and agrochemical research. The bromine substituent offers a reactive site for cross-coupling, while the trifluoromethyl group enhances lipophilicity.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 1g, 3-Bromo-7-azaindole, 95%, [74420-15-8], B10814 197.03 C7H5BrN2
Compound: 3-Bromo-7-azaindole
CAS#: 74420-15-8
MDL#: not listed
Background: A brominated azaindole used as a building block in pharmaceutical research. Azaindoles are privileged nitrogen heterocyclic scaffolds in drug discovery, and the bromine substituent provides a reactive site for cross-coupling functionalization.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 5g, 3-Bromo-7-azaindole, 95%, [74420-15-8], B10814 197.03 C7H5BrN2
Compound: 3-Bromo-7-azaindole
CAS#: 74420-15-8
MDL#: not listed
Background: A brominated azaindole used as a building block in pharmaceutical research. Azaindoles are privileged nitrogen heterocyclic scaffolds in drug discovery, and the bromine substituent provides a reactive site for cross-coupling functionalization.
Storage: Store at room temperature, under dry conditions.
Frontier Specialty Chemicals 25g, 4-Bromo-3-trifluoromethyl-1H-pyrazole, 98%, [19968-17-3], B10918 214.971 C4H2BrF3N2
Compound: 4-Bromo-3-trifluoromethyl-1H-pyrazole
CAS#: 19968-17-3
MDL#: not listed
Background: A brominated, trifluoromethylated pyrazole used as a building block in pharmaceutical and agrochemical research. The bromine substituent offers a reactive site for cross-coupling, while the trifluoromethyl group enhances lipophilicity.
Storage: Store at room temperature, under dry conditions.
Sigma Aldrich Fine Chemicals Biosciences 5-Bromophthalide 97% | 64169-34-2 | MFCD01797360 | 5G
5-Bromophthalide 97% | Purity: 97% | Mol Wt: 213.03 | 64169-34-2 | MFCD01797360 | 5G
Sigma Aldrich Fine Chemicals Biosciences 2-Bromo-5-hydroxypyrazine 95% | Purity: 95% | Mol Wt: 174.98 | 374063-92-0 | MFCD06245330 | 250MG
2-Bromo-5-hydroxypyrazine 95% | Purity: 95% | Mol Wt: 174.98 | 374063-92-0 | MFCD06245330 | 250MG
Sigma Aldrich Fine Chemicals Biosciences 2-Bromopyrimidine 95% | 4595-60-2 | MFCD00014601 | 1G
2-Bromopyrimidine 95% | Purity: 95% | Mol Wt: 158.98 | 4595-60-2 | MFCD00014601 | 1G
Sigma Aldrich Fine Chemicals Biosciences 2-Amino-6-bromobenzothiazole 97% | 15864-32-1 | MFCD00152229 | 1G
2-Amino-6-bromobenzothiazole 97% | Purity: 97% | Mol Wt: 229.1 | 15864-32-1 | MFCD00152229 | 1G
Sigma Aldrich Fine Chemicals Biosciences 4-Bromo-1-methyl-1H-pyrazole 97% | 15803-02-8 | MFCD02179565 | 5G
4-Bromo-1-methyl-1H-pyrazole 97% | Purity: 97% | Mol Wt: 161 | 15803-02-8 | MFCD02179565 | 5G
Sigma Aldrich Fine Chemicals Biosciences N-Boc-5-bromoindole 97% | 182344-70-3 | MFCD02090067 | 5G
N-Boc-5-bromoindole 97% | Purity: 97% | Mol Wt: 296.16 | 182344-70-3 | MFCD02090067 | 5G
Sigma Aldrich Fine Chemicals Biosciences 6-Bromo-1H-benzimidazole 97% | 4887-88-1 | MFCD00460014 | 1G
6-Bromo-1H-benzimidazole 97% | Purity: 97% | Mol Wt: 197.03 | 4887-88-1 | MFCD00460014 | 1G
Frontier Specialty Chemicals 1g, 5-Bromo-2-fluoropyrimidine, >98%, [62802-38-4], B10152 176.98 C4H2BrFN2
Compound: 5-Bromo-2-fluoropyrimidine
CAS#: 62802-38-4
MDL#: MFCD07787364
Background: A halogenated pyrimidine used as a biochemical reagent in proteomics research. The fluoride group supports nucleophilic aromatic substitution while the bromide group enables palladium-catalyzed carbon-carbon coupling, making this compound useful for constructing electron-pulling push-pull molecules.
Storage: Store at 2-8°C, under dry conditions.