Azetidine hydrochloride
97%
- Product Code: 122757
Alias:
Azetidine hydrochloride
CAS:
36520-39-5
| Molecular Weight: | 93.56 g./mol | Molecular Formula: | C₃H₇NHCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191762 | |
| Melting Point: | >300 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Azetidine hydrochloride is primarily used in organic synthesis as a building block for the creation of more complex chemical compounds. It serves as a precursor in the development of pharmaceuticals, particularly in the synthesis of beta-lactam antibiotics and other heterocyclic compounds. Its structure is valuable in medicinal chemistry for designing molecules with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in research settings to study ring strain and reactivity in small cyclic amines, aiding in the development of novel chemical reactions and methodologies.
Product Specification:
| Test | Specification |
|---|---|
| Carbon | 37.2-39.9 |
| Nitrogen | 14.4-15.5 |
| Purity (Neutralization Titration) | 96.5-100 |
| Appearance | White To Orange To Brown Powder, Crystals Or Chunks |
| Infrared Spectrum | Conforms To Structure |
| Melting Point | More Than 300 Degree Celsius |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿490.00 |
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| 5.000 | 10-20 days | ฿1,880.00 |
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| 25.000 | 10-20 days | ฿9,080.00 |
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| 100.000 | 10-20 days | ฿36,280.00 |
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Azetidine hydrochloride
Azetidine hydrochloride is primarily used in organic synthesis as a building block for the creation of more complex chemical compounds. It serves as a precursor in the development of pharmaceuticals, particularly in the synthesis of beta-lactam antibiotics and other heterocyclic compounds. Its structure is valuable in medicinal chemistry for designing molecules with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in research settings to study ring strain and reactivity in small cyclic amines, aiding in the development of novel chemical reactions and methodologies.
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