Benzyl (S,S,S)-2-azabicyclo[3.3.0]octane-3-carboxylate hydrochloride
97%
- Product Code: 60196
Alias:
(S,S,S)-2-Azabicyclo[3,3,0]octanecarboxylate benzyl ester hydrochloride; (S,S,S)-2-Azabicyclo[3,3,0] Benzyl octane-3-carboxylate hydrochloride
CAS:
87269-87-2
| Molecular Weight: | 281.78 g./mol | Molecular Formula: | C₁₅H₁₉NO₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04974076 | |
| Melting Point: | 176-180 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular disorders. Its unique bicyclic structure makes it valuable for designing drugs that interact with specific enzymes or receptors in the body. Additionally, it is employed in the preparation of chiral compounds, aiding in the study of stereochemistry and the development of enantiomerically pure drugs. Its application extends to medicinal chemistry, where it is used to explore new therapeutic agents with improved efficacy and reduced side effects.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Orange to Green powder to crystal |
| PURITY | 96.5-100 |
| SPECIFIC ROTATION A20DC1 DMSO | -32.0--28.0 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿600.00 |
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| 5.000 | 10-20 days | ฿1,860.00 |
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| 25.000 | 10-20 days | ฿9,260.00 |
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Benzyl (S,S,S)-2-azabicyclo[3.3.0]octane-3-carboxylate hydrochloride
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular disorders. Its unique bicyclic structure makes it valuable for designing drugs that interact with specific enzymes or receptors in the body. Additionally, it is employed in the preparation of chiral compounds, aiding in the study of stereochemistry and the development of enantiomerically pure drugs. Its application extends to medicinal chemistry, where it is used to explore new therapeutic agents with improved efficacy and reduced side effects.
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