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Product Line: Pharmaceutical Chemicals

1-tert-Butoxy-4-chlorobenzene

CAS 18995-35-2

Molecular structure of 1-tert-Butoxy-4-chlorobenzene

CAS · 18995-35-2

01

Product Overview

1-tert-Butoxy-4-chlorobenzene is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance Colorless and transparent liquid
Content 99% min
APHA 20 max
Moisture content 0.05% max
Toluene 0.1% max
Isobutylene 3-polymer 0.3% max
P-chlorophenol 0.05% max
High boiling point impurities 0.1% max
03

Applications

1-tert-Butoxy-4-chlorobenzene is an important aromatic intermediate frequently used in the synthesis of pharmaceuticals, agrochemicals, specialty chemicals, and advanced organic materials. Its structure, featuring both a tert-butoxy substituent and a chloro group on a benzene ring, provides useful reactivity patterns for further functionalization through substitution, coupling, or oxidation reactions. In pharmaceutical research, it serves as a precursor for the development of bioactive compounds, enabling the construction of molecular frameworks that demand electron-rich aromatic systems or sterically protected intermediates. In agrochemical synthesis, it helps form herbicides, fungicides, and plant-regulating agents, especially compounds requiring halogenated aromatic cores or bulky ether substituents to enhance environmental stability and biological activity. Additionally, the compound is used in the preparation of advanced polymers, liquid crystals, and materials where steric bulk and controlled aromatic substitution are essential to achieving specific thermal, mechanical, or optical properties. Its stability under typical reaction conditions makes it suitable for multi-step synthetic routes where reliable aromatic intermediates are needed.

04

Benefits

1-tert-Butoxy-4-chlorobenzene offers several advantages for chemists and product developers. The tert-butoxy group provides steric protection and electron-donating effects, which help modulate the reactivity of the aromatic ring and guide selective substitution or coupling reactions. This results in predictable behavior during synthesis and cleaner reaction pathways, reducing the formation of undesired byproducts. The chloro substituent serves as a versatile leaving group, facilitating cross-coupling processes such as Suzuki, Buchwald-Hartwig, or Ullmann reactions, which are essential for constructing complex functional molecules efficiently. The compound is chemically stable, easy to store, and compatible with a wide range of reagents and solvents, making it a convenient choice in laboratory and industrial settings. Its structural features also contribute to improved performance in final products, such as enhanced thermal stability in polymers or fine-tuned bioactivity in pharmaceutical and agrochemical derivatives. These characteristics collectively improve synthetic flexibility, optimize yields, and support the design of compounds with tailored physical and chemical properties.

05

Conclusion

1-tert-Butoxy-4-chlorobenzene is a valuable aromatic intermediate widely used across pharmaceutical research, agrochemical development, and advanced material synthesis. Its combination of a reactive chloro site and a stabilizing tert-butoxy group allows chemists to perform selective, predictable transformations, paving the way for efficient construction of complex organic structures. The compound's stability, reactivity, and compatibility with modern synthetic methodologies make it a reliable tool for creating high-performance chemicals and materials. Its continued relevance in diverse fields highlights its importance as a foundational building block in contemporary organic synthesis.

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