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Product Line: Pharmaceutical Chemicals

3-Methoxybenzoyl chloride

CAS 1711-05-3

Molecular structure of 3-Methoxybenzoyl chloride

CAS · 1711-05-3

01

Product Overview

3-Methoxybenzoyl chloride 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: Yellow to brownish yellow liquid
Purity (GC): 98% min
Water content: 0.5% max
Density: 1.20 ~ 1.30 g/ml
03

Applications

 

 

1. Intermediate in Organic Synthesis

Widely used as a building block for synthesizing a variety of organic compounds such as:

Pharmaceuticals

Agrochemicals

Dyes and pigments

Perfumes and fragrances

2. Acylation Reactions

Employed in Friedel-Crafts acylation and other acylation processes to introduce the 3-methoxybenzoyl group into aromatic or heterocyclic substrates.

3. Pharmaceutical Development

Used in the preparation of bioactive molecules with the 3-methoxybenzoyl moiety, which can contribute to desirable pharmacological properties such as anti-inflammatory or antimicrobial effects.

4. Synthesis of Esters and Amides

Reacts with alcohols and amines to form esters and amides, important in the creation of polymers, surfactants, and medicinal compounds.

5. Research Applications

Utilized in laboratories for the synthesis of novel compounds in medicinal chemistry and material science research.

04

Benefits

High Reactivity: Acid chloride functional group facilitates rapid and efficient acylation.

Versatile Intermediate: Enables synthesis of a wide range of chemical entities.

Structural Specificity: The methoxy substituent at the 3-position offers electronic effects that can influence biological activity or material properties.

Commercial Availability: Readily available from chemical suppliers, supporting research and production needs.

05

Conclusion

3-Methoxybenzoyl chloride (CAS 1711-05-3) is an important reactive intermediate in organic chemistry, valued for its role in acylation reactions and synthesis of functionalized compounds. Its combination of a reactive acid chloride group and a methoxy-substituted aromatic ring makes it essential in pharmaceutical, agrochemical, and materials research. Proper handling and storage are required due to its high reactivity and sensitivity to moisture.

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