3-Oxetanemethanol丨CAS 6246-06-6

3-Oxetanemethanol丨CAS 6246-06-6
Product Introduction:
Catalog No.: SS084220
CAS No.: 6246-06-6
Purity: 98%min
Product Name: 3-Oxetanemethanol
Molecular Formula: C4H8O2
Molecular Weight: 88.11
Synonym(s): Oxetan-3-ylmethanol
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Technical Parameters
Description

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Specifications of 3-Oxetanemethanol丨CAS 6246-06-6

 

Appearance:

Colorless to yellow liquid

HNMR:

Conforms

Purity:

98% min

The Largest Impurity:

1.0% max

Water:

1% max

 

Transport Information of 3-Oxetanemethanol丨CAS 6246-06-6

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2932999099117

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. -20 °C. Handle under nitrogen, protect from moisture. Store under nitrogen.

Condition to Avoid

Avoid contact with skin and eyes. Avoid inhalation of vapor or mist.

Package

 

 

Manufacturing Information of 3-Oxetanemethanol丨CAS 6246-06-6

 

Parameter

Specification

Capacity

100kg/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2015

Stock

 

 

 

 

Overview

3-Oxetanemethanol丨CAS 6246-06-6 is a heterocyclic compound characterized by a strained oxetane ring (a four-membered cyclic ether) with a hydroxymethyl side chain. This structure provides unique reactivity useful in organic synthesis and pharmaceutical chemistry.


 

Applications

1. Pharmaceutical Intermediate

Used as a building block in the synthesis of bioactive molecules and pharmaceuticals, especially in designing molecules with oxetane rings to enhance drug properties.

Oxetane rings are increasingly employed in medicinal chemistry to improve metabolic stability, aqueous solubility, and bioavailability of drugs.

2. Organic Synthesis

Serves as a versatile intermediate in synthetic routes for the preparation of complex molecules.

The reactive hydroxyl group (-CH2OH) enables further functionalization, while the strained oxetane ring can undergo ring-opening reactions under suitable conditions.

Employed in the synthesis of heterocycles, lactones, and other oxygen-containing frameworks.

3. Material Science

Potential use in polymer chemistry and materials science due to the strained ring system that can influence polymer properties when incorporated.


 

Benefits

1. Unique Structural Properties

The oxetane ring imparts ring strain, making it a useful reactive site in chemical transformations.

The presence of the hydroxymethyl group allows for versatile chemical modifications.

2. Enhances Drug-like Properties

Incorporation of oxetane rings into drug molecules can improve pharmacokinetics by increasing water solubility and metabolic stability compared to analogous structures.

3. Synthetic Flexibility

Its dual functional groups allow for selective reactions, making it a valuable scaffold in complex molecule synthesis.


 

Conclusion

3-Oxetanemethanol丨CAS 6246-06-6 is a valuable chemical intermediate notable for its strained oxetane ring and hydroxymethyl group. It is widely used in pharmaceutical and organic synthesis to develop molecules with enhanced stability and bioavailability. Its unique structure provides versatile chemical reactivity, making it an important building block in advanced synthetic and material chemistry.

 

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