4-Chlorobutanal Diethyl Acetal丨CAS 6139-83-9

4-Chlorobutanal Diethyl Acetal丨CAS 6139-83-9
Product Introduction:
Catalog No.: SS133659
CAS No.: 6139-83-9
Purity(by GC): 97%
Product Name: 4-Chlorobutanal diethyl acetal
Molecular Formula: C8H17ClO2
Molecular Weight: 180.67
Synonym(s): 4-Chloro-1,1-diethoxy-butane
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Technical Parameters
Description

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Specifications

 

Appearance Colorless to light yellow liquid
Purity (by GC) 97%
Water (KF) 1% max
Single impurity 1% max
Total impurity 3% max

 

 

 

Applications

 

4-Chlorobutanal diethyl acetal is primarily used as an intermediate in organic synthesis and pharmaceutical research. Its acetal-protected aldehyde functionality makes it useful for multi-step synthetic routes where selective reactivity is required. It serves as a precursor for preparing heterocycles, substituted amines, alcohol derivatives, and other fine chemicals. The compound is often applied in the synthesis of active pharmaceutical ingredients, agrochemicals, and specialty chemical building blocks. It is also utilized in polymer chemistry as a functional monomer precursor and in laboratory research for studying acetal chemistry, controlled deprotection strategies, and chlorinated intermediates.

 

Benefits

 

The benefits of 4-chlorobutanal diethyl acetal include its stability compared to the free aldehyde, allowing easier handling, storage, and transport. The acetal group protects the aldehyde during complex reaction sequences and can be selectively removed under mild acidic conditions, providing controlled access to the reactive aldehyde functionality when needed. Its chlorinated side chain offers versatile reactivity, enabling nucleophilic substitution and further functionalization. These properties make the compound a reliable and flexible intermediate in synthetic design, supporting high yields and reproducible results in diverse chemical transformations.

 

Conclusion

 

4-Chlorobutanal diethyl acetal is a valuable synthetic intermediate used in pharmaceutical, agrochemical, and fine chemical development. Its protected aldehyde group, combined with the reactive chlorinated chain, provides versatility and stability in multi-step synthesis. These characteristics make it an efficient and practical reagent for constructing complex molecules and advancing research and industrial applications.

 

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