(S)-2-Methyl-pyrrolidine
(S)-2-Methyl-pyrrolidine Basic information
- Product Name:
- (S)-2-Methyl-pyrrolidine
- Synonyms:
-
- (S)-(+)-2-METHYLPYRROLIDINE
- (S)-2-METHYL-PYRROLIDINE
- D-2-METHYLPYRROLIDINE
- METHYLPYRROLIDINE(S-2-)
- (2S)-2-Methylpyrrolidine
- 2-(S)-METHYLPYRROLIDINE
- (S)-(+)-2-Methylpyrrolidine 97%
- Pyrrolidine, 2-methyl-, (2S)-
- CAS:
- 59335-84-1
- MF:
- C5H11N
- MW:
- 85.15
- Product Categories:
-
- Chiral Building Blocks
- Heterocyclic Building Blocks
- Pyrrolidines
- Heterocyclic Series
- Chiral Compound
- Benzenes
- Mol File:
- 59335-84-1.mol
(S)-2-Methyl-pyrrolidine Chemical Properties
- Boiling point:
- 97-99 °C(lit.)
- Density
- 0.842 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.4354
- Flash point:
- 45 °F
- storage temp.
- 2-8°C
- pka
- 10.93±0.10(Predicted)
- Appearance
- Colorless to light yellow Liquid
- optical activity
- [α]20/D +19°, c = 5 in methanol
- CAS DataBase Reference
- 59335-84-1(CAS DataBase Reference)
Safety Information
- Hazard Codes
- F,C
- Risk Statements
- 11-22-34
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN 2924 3/PG 2
- WGK Germany
- 2
- Hazard Note
- Corrosive/Highly Flammable
- PackingGroup
- Ⅱ
- HS Code
- 2933998090
(S)-2-Methyl-pyrrolidine Usage And Synthesis
Synthesis
872-32-2
765-38-8
The general procedure for the synthesis of 2-methylpyrrolidine from 2-methylpyrroline was as follows: whole-cell biotransformation reactions were carried out at 30 °C in a shaker at 1000 rpm in a sodium phosphate buffer (100 mM, pH 7.0). Freshly harvested resting cells of E. coli BL21(DE3) expressing IRED with a final OD600nm value of 90 were used.The reaction mixture contained 2.5 or 5 mM of imine substrate and 50 mM of glucose as co-substrate.
References
[1] Organic and Biomolecular Chemistry, 2010, vol. 8, # 20, p. 4533 - 4535
[2] Bioscience, Biotechnology and Biochemistry, 2011, vol. 75, # 9, p. 1778 - 1782
[3] ChemBioChem, 2013, vol. 14, # 11, p. 1372 - 1379
[4] ChemCatChem, 2015, vol. 7, # 4, p. 579 - 583
[5] Journal of Molecular Catalysis B: Enzymatic, 2014, vol. 110, p. 126 - 132
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