Molecular structure of N-Boc-L-prolinol, CAS Number: 69610-40-8
N-Boc-L-prolinol (CAS 69610-40-8)
Alternate Names:
(S)-1-Boc-2-pyrrolidinemethanol
CAS Number:
69610-40-8
Molecular Weight:
201.26
Molecular Formula:
C10H19NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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This is used to synthesize anticoagulants. (5) Building block for novel nicotinic acetylcholine receptor ligands with cognition-enhancing properties. (1), (2), (3) This is also used in the synthesis of chiral -amino sulfides and -amino thiols. (4)
N-Boc-L-prolinol (CAS 69610-40-8) References
- 4-Phenylbutanoyl-2(S)-acylpyrrolidines and 4-phenylbutanoyl-L-prolyl-2(S)-acylpyrrolidines as prolyl oligopeptidase inhibitors. | Wallén, EA., et al. 2002. Bioorg Med Chem. 10: 2199-206. PMID: 11983517
- Recent Advances in Asymmetric Synthesis of Pyrrolidine-Based Organocatalysts and Their Application: A 15-Year Update. | Quintavalla, A., et al. 2023. Molecules. 28: PMID: 36903480
- Novel 3-Pyridyl ethers with subnanomolar affinity for central neuronal nicotinic acetylcholine receptors. | Abreo, MA., et al. 1996. J Med Chem. 39: 817-25. PMID: 8632405
- Structure-activity studies on 2-methyl-3-(2(S)-pyrrolidinylmethoxy) pyridine (ABT-089): an orally bioavailable 3-pyridyl ether nicotinic acetylcholine receptor ligand with cognition-enhancing properties. | Lin, NH., et al. 1997. J Med Chem. 40: 385-90. PMID: 9022806
- Synthesis, characterisation, cytotoxicity and radioprotective effect of novel chiral nitronyl nitroxyl radicals | Qin, X. Y., Ding, G. R., Wang, X. W., Tan, J., Guo, G. Z., & Sun, X. L. 2009. Journal of Chemical Research. 2009(8): 511-514.
- Chiral quaternary alkylammonium ionic liquid [Pro-dabco][BF4]: as a recyclable and highly efficient organocatalyst for asymmetric Michael addition reactions | Xu, D. Z., Liu, Y., Shi, S., & Wang, Y. 2010. Tetrahedron: Asymmetry. 21(20): 2530-2534.
- Synthesis of Enantiomerically Pure Nitronyl Nitroxide Radicals Through Chiral Pool | Qin, X. Y., Ma, Y., Wang, Q. F., Wang, C., Sun, X. L., & Liu, P. 2012. Letters in Organic Chemistry. 9(5): 314-319.
- Synthesis and biological activity evaluation of dolastatin 10 analogues with N-terminal modifications | Wang, X., Dong, S., Feng, D., Chen, Y., Ma, M., & Hu, W. 2017. Tetrahedron. 73(16): 2255-2266.
- Larger scale Stahl oxidation with instant Cu removal in convenient synthesis of chiral bidentate N–heterocyclic carbene precursor | Grudzień, K., Nogaś, W., Szczepaniak, G., & Grela, K. 2021. Polyhedron. 199: 115090.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N-Boc-L-prolinol, 1 g | sc-255347 | 1 g | $61.00 |