Description

2′-Bromo-5′-phenyl-1,1′:3′,1”-terphenyl (CAS No. 10368-73-7) is a high-purity brominated terphenyl derivative with the molecular formula C₂₄H₁₇Br. This compound is widely utilized in organic synthesis, material science, and pharmaceutical research due to its unique structural properties and reactivity. The aromatic bromine substituent enhances its utility as a versatile intermediate in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings. With exceptional thermal stability and a well-defined crystalline structure, this compound is ideal for advanced research applications requiring precise molecular architectures. Available in rigorously tested batches, it is supplied with comprehensive analytical data (HPLC, NMR, MS) to ensure consistency and reliability for your scientific investigations.

Properties

• CAS Number: 10368-73-7
• Complexity: 359
• IUPAC Name: 2-bromo-1,3,5-triphenyl-benzene
• InChI: InChI=1S/C24H17Br/c25-24-22(19-12-6-2-7-13-19)16-21(18-10-4-1-5-11-18)17-23(24)20-14-8-3-9-15-20/h1-17H
• InChI Key: JQAGNDRJKSDTEU-UHFFFAOYSA-N
• Exact Mass: 384.05136
• Molecular Formula: C24H17Br
• Molecular Weight: 385.3
• SMILES: C1=CC=C(C=C1)C2=CC(=C(C(=C2)C3=CC=CC=C3)Br)C4=CC=CC=C4
• Monoisotopic Mass: 384.05136
• Synonyms: 2′-Bromo-5′-phenyl-1,1′:3′,1”-terphenyl, 659-706-8, 10368-73-7, 2-bromo-1,3,5-triphenylbenzene, 2-bromo-1,3,5-triphenyl-benzene, 1-BROMO-2,4,6-TRIPHENYLBENZENE, 2,4,6-Triphenylbromobenzene, MFCD00092320, NSC157786, SCHEMBL1328447, YSZC1492, DTXSID40303300, 2′-Bromo-5′-phenyl-m-terphenyl, AKOS024432746, NSC-157786, BS-14250, SY046150, DB-148771, B5674, CS-0163437, F18704, 2 inverted exclamation mark -Bromo-5 inverted exclamation mark -phenyl-1,1 inverted exclamation mark :3 inverted exclamation mark ,1 inverted exclamation mark inverted exclamation mark -terphenyl

2′-Bromo-5′-phenyl-1,1′:3′,1”-terphenyl serves as a key intermediate in the synthesis of liquid crystals, OLED materials, and pharmaceutical scaffolds. Its bromine functionality enables efficient palladium-catalyzed cross-coupling reactions for constructing complex conjugated systems. Researchers also employ it in supramolecular chemistry and polymer science to modify electronic properties of organic semiconductors. Suitable for controlled functionalization in optoelectronic device fabrication.

Safety and Hazards

GHS Hazard Statements

• H302 (97.4%): Harmful if swallowed [Warning Acute toxicity, oral]
• H319 (97.4%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

• P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P330, P337+P317, and P501

Hazard Classes and Categories

• Acute Tox. 4 (97.4%)
• Eye Irrit. 2 (97.4%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.