Product Name :
2-Methylpyrrolidine (CAS 765-38-8)

Synonym :

Application :

CAS:
765-38-8

Purity:

Molecular Weight:
85.15

Formula :
C5H11N

Physical state:
Liquid

solubility :

Shipping Condition :
Store at room temperature

Melting point:
-90° C

SMILES:
CC1CCCN1

References:
:Efficient and practical synthesis of (R)-2-methylpyrrolidine. | Zhao, D., et al. 2006. J Org Chem. 71: 4336-8. PMID: 16709084Modeling proline ligation in the heme-dependent CO sensor, CooA, using small-molecule analogs. | Pinkert, JC., et al. 2006. J Biol Inorg Chem. 11: 642-50. PMID: 16724227In vitro SAR of pyrrolidine-containing histamine H3 receptor antagonists: trends across multiple chemical series. | Nersesian, DL., et al. 2008. Bioorg Med Chem Lett. 18: 355-9. PMID: 18077160[Regioselectivity in the dehydrogenation of substituted ethylenediamines as nicotine models]. | Möhrle, H. and Berlitz, J. 2009. Pharmazie. 64: 565-73. PMID: 19827296Extraction of Teucrium manghuaense and evaluation of the bioactivity of its extract.5-Bromo-7-chloro-1H-indole Chemscene | Yin, G., et al. 2009. Int J Mol Sci. 10: 4330-41. PMID: 20057948Asymmetric synthesis of chiral cyclic amine from cyclic imine by bacterial whole-cell catalyst of enantioselective imine reductase. | Mitsukura, K., et al. 2010. Org Biomol Chem. 8: 4533-5. PMID: 20820664Purification and characterization of a novel (R)-imine reductase from Streptomyces sp. GF3587. | Mitsukura, K., et al. 2011. Biosci Biotechnol Biochem. 75: 1778-82. PMID: 21897027Structure and activity of NADPH-dependent reductase Q1EQE0 from Streptomyces kanamyceticus, which catalyses the R-selective reduction of an imine substrate. | Rodríguez-Mata, M., et al. 2013. Chembiochem. 14: 1372-9. PMID: 238138532-Methyl-4-(naphthalen-2-yl)-3a-nitro-3,3a,4,9b-tetra-hydro-2H-spiro-[chromeno[3,4-c]pyrrole-1,3′-indolin]-2′-one. | Devi, SK., et al. 2013. Acta Crystallogr Sect E Struct Rep Online. 69: o1045-6.Formula of 4-Bromo-2-methylpyrimidine PMID: 24046621Structure, Activity and Stereoselectivity of NADPH-Dependent Oxidoreductases Catalysing the S-Selective Reduction of the Imine Substrate 2-Methylpyrroline.PMID:33559099 | Man, H., et al. 2015. Chembiochem. 16: 1052-9. PMID: 25809902Polymorphic chiral squaraine crystallites in textured thin films. | Zablocki, J., et al. 2020. Chirality. 32: 619-631. PMID: 32155676Optical Activity in Saturated Cyclic Amines: Untangling the Roles of Nitrogen-Inversion and Ring-Puckering Dynamics. | Craft, CL., et al. 2021. J Phys Chem A. 125: 5562-5584. PMID: 34142836Acylative kinetic resolution of racemic methyl-substituted cyclic alkylamines with 2,5-dioxopyrrolidin-1-yl (R)-2-phenoxypropanoate. | Gruzdev, DA., et al. 2022. Org Biomol Chem. 20: 862-869. PMID: 35006228Synthesis of Chiral Covalent Organic Frameworks via Asymmetric Organocatalysis for Heterogeneous Asymmetric Catalysis. | Li, F., et al. 2022. Angew Chem Int Ed Engl. 61: e202115044. PMID: 35357070