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Atomfair 4-Bromotoluene p-Bromotoluene C7H7Br
Description 4-Bromotoluene (CAS No. 106-38-7), also known as p-Bromotoluene or 1-Bromo-4-methylbenzene , is a high-purity aromatic organic compound with the molecular formula C7H7Br. This colorless to pale yellow liquid is widely utilized in synthetic organic chemistry, pharmaceutical intermediates, and material science research. With a boiling point of 184-185??C and a melting point of 26-28??C, it exhibits excellent solubility in organic solvents like ethanol, ether, and benzene while being insoluble in water. Packaged under inert conditions to ensure stability, our 4-Bromotoluene is rigorously tested via GC/HPLC to meet ??98% purity standards, making it ideal for precise laboratory applications. Suitable for use…
Description
Description
4-Bromotoluene (CAS No. 106-38-7), also known as p-Bromotoluene or 1-Bromo-4-methylbenzene, is a high-purity aromatic organic compound with the molecular formula C7H7Br. This colorless to pale yellow liquid is widely utilized in synthetic organic chemistry, pharmaceutical intermediates, and material science research. With a boiling point of 184-185??C and a melting point of 26-28??C, it exhibits excellent solubility in organic solvents like ethanol, ether, and benzene while being insoluble in water. Packaged under inert conditions to ensure stability, our 4-Bromotoluene is rigorously tested via GC/HPLC to meet ??98% purity standards, making it ideal for precise laboratory applications. Suitable for use as a versatile building block in Grignard reactions, Suzuki couplings, and other cross-coupling methodologies.
- CAS No: 106-38-7
- Molecular Formula: C7H7Br
- Molecular Weight: 171.03
- Exact Mass: 169.97311
- Monoisotopic Mass: 169.97311
- IUPAC Name: 1-bromo-4-methylbenzene
- SMILES: CC1=CC=C(C=C1)Br
- Synonyms: 4-BROMOTOLUENE, 106-38-7, p-Bromotoluene, 1-Bromo-4-methylbenzene, Benzene, 1-bromo-4-methyl-
Application
4-Bromotoluene serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and liquid crystals. It is frequently employed in palladium-catalyzed cross-coupling reactions (e.g., Suzuki-Miyaura) to construct biaryl scaffolds. Researchers also utilize it to introduce bromomethyl groups into molecular systems for further functionalization. Its stability and reactivity make it valuable in organometallic chemistry and polymer research.
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