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Description
TCI C2233 2-(4-Chlorophenyl)ethanol is an aromatic alcohol belonging to the group of non-heterocyclic building blocks — small-molecule starting materials used as the point of departure for constructing larger chemical structures. Its molecule combines a chlorine-substituted benzene ring with a short ethanol chain, presenting two reactive sites within a single framework. In organic synthesis laboratories, materials of this kind form the backbone of daily work, because researchers can convert the hydroxyl group into esters, ethers, halides, or aldehydes according to the requirements of the reaction pathway being developed.
The characteristic that makes this compound a frequent choice is the balance between its reactivity and its stability. The primary hydroxyl group on the side chain is relatively easy to activate without demanding extreme reaction conditions, while the chlorine atom at the para position remains intact throughout the transformation and at the same time provides a handle for cross-coupling reactions in a later stage. This combination gives researchers good control over the sequence in which reactions are carried out, allowing one site to be addressed while the other is held in reserve.
In Indonesian laboratories, this compound is typically encountered in university organic chemistry research groups, in method development work, and in exploratory synthesis where routes are still being optimised. The small 5 g and 25 g pack sizes offered by TCI make it easier to match the quantity of material to the scale of the work at hand, which suits trial reactions and small-batch preparations rather than production-scale consumption.
Laboratory Applications
Multistep organic synthesis — serves as a compact starting framework whose two reactive sites let researchers build larger target structures through a planned sequence of transformations.
Functional group conversion studies — the primary hydroxyl can be transformed into esters, ethers, halides, or aldehydes, making it a practical substrate for exploring derivatisation routes.
Cross-coupling chemistry — the para-chlorine substituent survives earlier transformations and remains available as a handle for coupling reactions carried out at a later stage.
Reaction methodology development — its balance of reactivity and stability allows activation under moderate conditions, which suits laboratories testing and refining new synthetic procedures.
Academic research and teaching synthesis — small pack sizes and predictable reactivity make it suitable for university research groups running exploratory reactions on a modest scale.
Specifications
Brand: TCI
CAS number: 1875-88-3
Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Chemical class: aromatic alcohol, non-heterocyclic building block
Pack sizes: 5 g and 25 g
Storage: keep in the closed original container, following the storage conditions stated on the manufacturer's label and safety data sheet
Handling and Storage
Store the material in its original tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and ignition sources. Keep it separated from strong oxidising agents and other incompatible chemicals. Because this is an aromatic alcohol with a reactive hydroxyl group, containers should be resealed promptly after use to limit exposure to atmospheric moisture. Handle in a fume hood while wearing safety goggles, chemical-resistant gloves, and a laboratory coat. Always consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable chemical waste procedures.
