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[4-(Chloromethyl)phenyl]methanol is a versatile organic building block widely used in laboratory synthesis. Its molecular structure, featuring a chloromethyl group on a phenyl ring, makes it highly reactive in various chemical reactions such as substitution, addition, and catalytic processes. This compound is commonly utilized in the development of new heterocyclic compounds and complex organic structures. Its polarity and solubility in organic solvents like ethyl acetate and acetone further enhance its applicability in diverse chemical applications. In Indonesia, it is a key material for research in pharmaceuticals, industrial chemicals, and advanced materials, supporting both academic and industrial innovation.
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- Grzegozek et al. (2004). Regioselectivity in SNH Reactions of Some 3‐Nitro‐1,5‐naphthyridines with Chloromethyl Phenyl Sulfone.. ChemInform doi:10.1002/chin.200440151
- Arai et al. (2002). Asymmetric Darzens reaction utilizing chloromethyl phenyl sulfone under phase-transfer catalyzed conditions. Tetrahedron doi:10.1016/s0040-4020(01)01244-3
- Arai et al. (2002). ChemInform Abstract: Asymmetric Darzens Reaction Utilizing Chloromethyl Phenyl Sulfone under Phase‐Transfer Catalyzed Conditions.. ChemInform doi:10.1002/chin.200229041
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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