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CAS RN: 87269-87-2 | Product Number: B5344
Benzyl (S,S,S)-2-Azabicyclo[3.3.0]octane-3-carboxylate Hydrochloride
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![Benzyl (S,S,S)-2-Azabicyclo[3.3.0]octane-3-carboxylate Hydrochloride](/_ui/responsive/theme-tci/images/missing_product_zoom.jpg "Benzyl (S,S,S)-2-Azabicyclo[3.3.0]octane-3-carboxylate Hydrochloride")
Purity: >98.0%(T)(HPLC)
Synonyms:
- (S,S,S)-2-Azabicyclo[3.3.0]octane-3-carboxylic Acid Benzyl Ester Hydrochloride
Product Documents:
| Size | Unit Price | Hyderabad | Japan* | Quantity |
|---|---|---|---|---|
| 1G |
₹4,300.00
|
Contact Us | 1 |
|
| 5G |
₹11,800.00
|
5 | 15 |
|
*Upon orders receipt, Hyderabad stocks will be dispatched on the same day.
*Items available in Japan warehouse will be dispatched in 10-12 working days.
*INR price is exclusive of domestic taxes applicable.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | B5344 |
| Purity / Analysis Method | >98.0%(T)(HPLC) |
| Molecular Formula / Molecular Weight | C__1__5H__1__9NO__2·HCl = 281.78 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| CAS RN | 87269-87-2 |
| Reaxys Registry Number | 3636474 |
| PubChem Substance ID | 354334662 |
| MDL Number | MFCD04974076 |
Specifications
| Appearance | White to Orange to Green powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Argentometric Titration) | min. 98.0 % |
| Specific rotation [a]20/D | -28.0 to -32.0 deg(C=1, DMSO) |
Properties (reference)
| Melting Point | 181 °C |
| Specific Rotation | -31° (C=1,DMSO) |
| Solubility (soluble in) | Methanol |
GHS
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Application
A Synthetic Intermediate of Ramipril
This reagent is used for the synthesis of ramipril (Hoe 498) [CAS: 87333-19-5][R0219], an ACE inhibitor.
References
- Synthesis of unnatural amino acids: (S,S,S)-2-azabicyclo[3.3.0]octane-3-carboxylic acid
- Synthesis of a highly active angiotensin converting enzyme inhibitor: 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2-azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498)
- Asymmetric synthesis of (S,S,S)-2-aza-bicyclo[3.3.0]octane-3-carboxylic acid benzyl ester. Formal synthesis of ramipril
PubMed Literature
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