Molecular structure of (S)-(+)-2-(Anilinomethyl)pyrrolidine, CAS Number: 64030-44-0
(S)-(+)-2-(Anilinomethyl)pyrrolidine (CAS 64030-44-0)
CAS Number:
64030-44-0
Molecular Weight:
176.26
Molecular Formula:
C11H16N2
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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(S)-(+)-2-(Aminomethyl)pyrrolidine is a chiral vicinal diamine. The compound can be synthesized by reacting allyl chloride with ammonia and reducing the resulting allyl amine. This reaction requires high temperatures. Catalytic asymmetric and uses hydrogen chloride as a catalyst. (S)-(+)-2-(Aminomethyl)pyrrolidine can be used as an organocatalyst, for the asymmetric transformation of (S)-alanine or the asymmetric α-fluorination of linear and branched aldehydes using N-fluorobenzenesulfonamide as the fluorinating agent.
(S)-(+)-2-(Anilinomethyl)pyrrolidine (CAS 64030-44-0) References
- A ruthenium(II) complex with p-cymene and (S)-2-(anilinomethyl)pyrrolidine. | Aitali, M., et al. 2000. Acta Crystallogr C. 56 (Pt 9): 1088-9. PMID: 10986491
- Asymmetric synthesis of biaryl atropisomers by dynamic resolution on condensation of biaryl aldehydes with (-)-ephedrine or a proline-derived diamine. | Bracegirdle, A., et al. 2008. Beilstein J Org Chem. 4: 47. PMID: 19190743
- Comprehensive Profiling and Inheritance Patterns of Metabolites in Foxtail Millet. | Li, S., et al. 2018. Front Plant Sci. 9: 1716. PMID: 30542359
- Dissecting Heterosis During the Ear Inflorescence Development Stage in Maize via a Metabolomics-based Analysis. | Shi, X., et al. 2019. Sci Rep. 9: 212. PMID: 30659214
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(S)-(+)-2-(Anilinomethyl)pyrrolidine, 1 g | sc-250938 | 1 g | $131.00 |