Description

2-([1,1′-Biphenyl]-4-yl)-4-chloro-6-phenyl-1,3,5-triazine (CAS No. 1472062-94-4) is a high-purity organic compound with the molecular formula C₂₁H₁₄ClN₃. This chlorinated triazine derivative features a biphenyl and phenyl substitution pattern, making it a valuable intermediate in organic synthesis and materials science. Its IUPAC name is 2-chloro-4-phenyl-6-(4-phenylphenyl)-1,3,5-triazine, and it is characterized by its crystalline solid form, high thermal stability, and reactivity as a halogenated triazine. Suitable for research in pharmaceuticals, agrochemicals, and advanced materials, this compound is rigorously tested for quality and consistency. Available in customizable quantities with detailed analytical data (HPLC, NMR, MS) upon request.

Properties

• CAS Number: 1472062-94-4
• Complexity: 398
• IUPAC Name: 2-chloro-4-phenyl-6-(4-phenylphenyl)-1,3,5-triazine
• InChI: InChI=1S/C21H14ClN3/c22-21-24-19(17-9-5-2-6-10-17)23-20(25-21)18-13-11-16(12-14-18)15-7-3-1-4-8-15/h1-14H
• InChI Key: JKHCVYDYGWHIFJ-UHFFFAOYSA-N
• Exact Mass: 343.0876252
• Molecular Formula: C21H14ClN3
• Molecular Weight: 343.8
• SMILES: C1=CC=C(C=C1)C2=CC=C(C=C2)C3=NC(=NC(=N3)C4=CC=CC=C4)Cl
• Topological: 38.7
• Monoisotopic Mass: 343.0876252
• Synonyms: 1472062-94-4, 2-([1,1′-Biphenyl]-4-yl)-4-chloro-6-phenyl-1,3,5-triazine, 2-{[1,1′-BIPHENYL]-4-YL}-4-CHLORO-6-PHENYL-1,3,5-TRIAZINE, 2-((1,1′-Biphenyl)-4-yl)-4-chloro-6-phenyl-1,3,5-triazine, 878-389-9, 2-Chloro-4-(biphenyl-4-yl)-6-phenyl-1,3,5-triazine, 2-[1,1′-Biphenyl]-4-yl-4-chloro-6-phenyl-1,3,5-triazine, 1,3,5-Triazine, 2-[1,1′-biphenyl]-4-yl-4-chloro-6-phenyl-, 2-chloro-4-phenyl-6-(4-phenylphenyl)-1,3,5-triazine, 2-(BIPHENYL-4-YL)-4-CHLORO-6-PHENYL-1,3,5-TRIAZINE, 2-(4-Biphenylyl)-4-chloro-6-phenyl-1,3,5-triazine, MFCD27979856, SCHEMBL16332656, JKHCVYDYGWHIFJ-UHFFFAOYSA-N, AKOS027252156, SB22146, AS-70288, DA-10112, SY122040, B5792, CS-0054571, Biphenyl]-4-yl)-4-chloro-6-phenyl-1,3,5-triazine, 2-([1,1′-biphenyl]-4-yl)-4-chloro-6-phenyl-1,3,5-triazine

Application

This compound serves as a versatile building block in the synthesis of functionalized triazines for pharmaceutical and agrochemical applications. It is particularly useful in cross-coupling reactions to create complex heterocyclic systems. Researchers also explore its potential in optoelectronic materials due to its conjugated aromatic structure. Its reactivity as a chlorotriazine makes it valuable in polymer and supramolecular chemistry.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

• P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364

Hazard Classes and Categories

• Skin Irrit. 2 (100%)
• Eye Irrit. 2 (100%)

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