Hoffer's Chlorosugar丨CAS 4330-21-6

Hoffer's Chlorosugar丨CAS 4330-21-6
Product Introduction:
Catalog No.: SS120643
CAS No.: 4330-21-6
Purity: 95%min
Product Name: Hoffer's chlorosugar
Molecular Formula: C21H21ClO5
Molecular Weight: 388.8
Synonym(s): 2-Deoxy-alpha-D-erythropentofuranosyl chloride 3,5-bis(4-methylbenzoate)
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Technical Parameters
Description

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Specifications

 

Appearance off white powder
Purity 95% min
Loss on drying 2.0% max
Residue on Ignition 0.5% max

 

Transport Information

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2932190090303

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

-20℃

Condition to Avoid

 

Package

 

 

 

 

Applications

 

Hoffer's chlorosugar is primarily used as a key intermediate in carbohydrate chemistry and glycoside synthesis. It serves as a versatile building block for preparing various protected sugar derivatives, glycosyl donors, and analogs in the synthesis of complex oligosaccharides, glycoconjugates, and natural products. The compound is widely employed in medicinal chemistry for designing carbohydrate-based drugs and vaccines, as well as in chemical biology to study carbohydrate–protein interactions. Additionally, it finds use in the preparation of stereochemically defined sugar molecules essential for enzymatic and synthetic applications.

 

Benefits

 

Hoffer's chlorosugar offers high stereochemical control and reactivity, enabling selective glycosylation reactions under mild conditions. Its chlorinated functionality facilitates the formation of glycosidic bonds with excellent yield and regioselectivity. This intermediate simplifies the synthesis of complex sugars and glycoconjugates by reducing the number of protection/deprotection steps. Its use accelerates research in carbohydrate-based therapeutics and diagnostics by providing reliable access to structurally precise sugar building blocks.

 

Conclusion

 

Hoffer's chlorosugar is a crucial intermediate in carbohydrate synthesis, enabling efficient and selective construction of complex sugar molecules. Its stereochemical precision and reactivity support advances in drug discovery, vaccine development, and chemical biology, making it indispensable for modern carbohydrate chemistry.

 

 

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