TCI C0973 2-Chlorobenzyl Alcohol (CAS 17849-38-6) is an ortho-chlorinated benzylic alcohol supplied in a 25 g pack. Its benzylic hydroxyl group is readily oxidized or converted into a leaving group, while the aryl chloride offers a handle for further aromatic functionalization. These complementary reactive sites make it a practical branch point in multi-step synthetic routes for pharmaceutical and agrochemical research. Handle it in a fume hood with gloves and eye protection, and store it tightly closed in a cool, dry, light-protected place.
Related TCI products
- TCI B3946 149965-40-2 5-Bromo-2-chlorobenzyl Alcohol
- TCI C0650 873-63-2 3-Chlorobenzyl Alcohol
- TCI C0565 873-76-7 4-Chlorobenzyl Alcohol
- TCI T1884 4084-38-2 2,3,5,6-Tetrafluorobenzyl Alcohol
- TCI T1883 53072-18-7 2,3,4,5-Tetrafluorobenzyl Alcohol
- TCI T1204 32974-36-0 Pentafluorobenzyl p-Toluenesulfonate [Derivatizing Reagent for GC of Inorganic Anions]
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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
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
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5-Bromo-2-chlorobenzylAlcohol TCI B3946
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2,3,5,6-TetrafluorobenzylAlcohol TCI T1884
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3-Bromo-2-fluorobenzylAlcohol TCI B5143
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4-Bromo-2,6-difluorobenzylAlcohol TCI B5090
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