N-BOC- L- prolinol
Also known as tert-butyl (S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate, tert-butyl (2S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate, (S)-1-Boc-2-pyrrolidinemethanol
- CAS number
- 69610-40-8
- Molecular formula
- C10H19NO3
- Molecular weight
- 201.26 g/mol
- Catalogue number
- OS-23492
- Purity
- 99 %
- Grade
- Agricultural, Technical
- Form
- Powder
- Packing
- 25 kg
₹900 per kg
Documents
- Certificate of analysis (COA) On request
- Safety data sheet (MSDS) On request
Specifications
| CAS number | 69610-40-8 |
|---|---|
| Molecular formula | C10H19NO3 |
| Molecular weight | 201.26 g/mol |
| IUPAC name | tert-butyl (2S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate |
| InChIKey | BFFLLBPMZCIGRM-QMMMGPOBSA-N |
| SMILES | CC(C)(C)OC(=O)N1CCC[C@H]1CO |
| MDL number | MFCD00066232 |
| PubChem CID | 643448 |
| Physical form | Powder |
|---|
| Purity | 99 % |
|---|---|
| Grade | Agricultural, Technical |
| Packaging size | 25 kg |
|---|---|
| Packaging type | Bag |
Description and applications
N-Boc-L-prolinol is a chiral proline derivative that has been modified with an allyl group. It is a potent nicotinic acetylcholine antagonist, and it has been shown to have immune functions in vitro. The synthesis of N-Boc-L-prolinol occurs through a three-step process involving the use of organocatalysts, asymmetric synthesis, and stereoselective reactions. This molecule is also useful for the study of apoptotic signaling pathways in cells.
Applications
- Agriculture
- Farming
- Fermentation
- Human Nutrition
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