1-(3-Chloropropoxy)-4-methoxybenzene

GTC-023

Ethers

1-(3-Chloropropoxy)-4-methoxybenzene

CAS No.
1716-42-3
Catalogue ID
GTC-023

1-(3-Chloropropoxy)-4-methoxybenzene, CAS 1716-42-3. Source-derived identification, physical data and applications are provided for catalogue reference; request the current specification, COA and SDS for the required grade.

Catalogue aliases / related identifiers

4-(3-Chloropropoxy)anisole; 1-methoxy-4-(3-chloropropoxy)benzene; Benzene, 1-(3-chloropropoxy)-4-methoxy-; p-(3-Chloropropoxy)anisole; 4-Methoxyphenyl 3-chloropropyl ether; 1-(3-Chloropropoxy)-4-methoxy benzene; 4-(3-Chloropropoxy)-1-methoxybenzene

Supplied catalogue source: GTC-023 · Page 103

Reference data — confirm before ordering or use

The information below is a structured migration from the supplied catalogue snapshot. It is not a current product specification, COA or SDS. Confirm the actual supplier, grade, batch documents, classification, packing and destination requirements for your enquiry.

1-(3-Chloropropoxy)-4-methoxybenzene (CAS 1716-42-3) is a bifunctional aromatic ether featuring a reactive chloropropyl chain attached to a methoxy-substituted benzene ring. This structure makes it a valuable alkylating agent in organic synthesis for the construction of longer-chain aryloxy derivatives.


Basic Information

CAS No.1716-42-3
EC No.Not available
Linear FormulaC10H13ClO2
Molecular Weight200.66
AppearanceColorless to light yellow clear liquid
SolubilitySoluble in common organic solvents
Storage ConditionsStore in a tightly closed container in a cool, dry place. Protect from moisture and light.
Chemical StructureMolecular Structure of 1-(3-Chloropropoxy)-4-methoxybenzene

Key Applications

  • Reactive alkylation intermediate: 1-(3-Chloropropoxy)-4-methoxybenzene serves as an effective alkylating agent for introducing the 3-(4-methoxyphenoxy)propyl group into target molecules. It is relevant to Alkoxy Propanols and Propylene Glycol Ethers for Pharmaceutical Synthesis, where alkoxy-functional intermediates enable controlled chain extension and functionalization.

  • Chloroalkyl functionalization: The terminal chloride group provides a reactive site for nucleophilic substitution, allowing further derivatization into amines, ethers, or other functional groups. This reactivity is part of the broader  alkoxy ether application category.

  • Fine chemical intermediate: Used in the synthesis of specialty chemicals and pharmaceutical intermediates, particularly where stepwise functional group transformation is required.

  • Aromatic compound synthesis: Facilitates the preparation of substituted aromatic systems through nucleophilic substitution and side-chain modification, supporting the development of advanced functional molecules.

  • Laboratory research: Applied in research for synthetic route development, linker design, and exploration of bioactive molecule candidates involving aryl ether structures.

  • Process development: Supports route optimization and scale-up in processes requiring reliable chloroalkyl aryl ether intermediates with consistent reactivity.

1-(3-Chloropropoxy)-4-methoxybenzene belongs to the Alkoxy Propanols & Glycol Ethers application category and is part of our broader portfolio of Ethers for Pharmaceutical Intermediates & Specialty Synthesis, covering alkoxy-functional intermediates, reactive linkers, and ether-based building blocks for API and fine chemical synthesis.


  • Flexible global supply: Established international logistics networks ensure stable supply from laboratory to bulk scale for fine chemical customers worldwide.

  • SDS and COA support: Full SDS, COA, and supporting technical documentation provided upon request to facilitate quality review and regulatory compliance.

  • Packaging and technical service: Flexible packaging options including 25L/200L HDPE drum, supported by responsive technical communication for synthesis needs.

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