TCI C0650 3-Chlorobenzyl Alcohol is a meta-substituted benzyl alcohol that combines a benzylic hydroxyl group with an aromatic chlorine handle. The hydroxyl group is readily converted into halides, ethers, esters, aldehydes, or carboxylic acids using well-established transformations. The chlorine substituent offers an additional site for transition-metal catalysed cross-coupling, allowing rapid elaboration into more complex aromatic frameworks. AMI Scientific offers this TCI building block in a convenient 10 mL pack for laboratory-scale synthesis in medicinal and agrochemical research.
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- Fukui et al. (2016). Meerwein–Ponndorf–Verley-type Reduction over a Metal-free TiO2 Photocatalyst in Alcohol: Chemoselective Hydrogenation of Chlorobenzaldehyde to Chlorobenzyl Alcohol. Chemistry Letters doi:10.1246/cl.160476
- Deori et al. (2015). (100) surface-exposed CeO 2 nanocubes as an efficient heterogeneous catalyst in the tandem oxidation of benzyl alcohol, para-chlorobenzyl alcohol and toluene to the corresponding aldehydes selectively. Journal of Materials Chemistry A doi:10.1039/c4ta06547f
- Niki et al. (1996). A Pulsed 35Cl NQR Study on the Molecular Motions and Phase Transition of 4-Chlorobenzyl Alcohol. Zeitschrift für Naturforschung A doi:10.1515/zna-1996-5-662
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