679097
(R)-(−)-2-Methylpyrrolidine
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About This Item
Empirical Formula (Hill Notation):
C5H11N
CAS Number:
Molecular Weight:
85.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
InChI
1S/C5H11N/c1-5-3-2-4-6-5/h5-6H,2-4H2,1H3/t5-/m1/s1
SMILES string
C[C@@H]1CCCN1
InChI key
RGHPCLZJAFCTIK-RXMQYKEDSA-N
refractive index
n20/D 1.4353
density
0.842 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
Related Categories
Application
(R)-(−)-2-Methylpyrrolidine, an optically active amine that can be used as a key building block to synthesize:
- 4,5-fused pyridazinone derivatives are applicable as potent histamine H3 receptor antagonists.
- Naphthalenoid histamine H3 receptor antagonist.
- Pyrrolo[2,3-d]pyrimidine derivatives as potent inhibitors of leucine-rich repeat kinase 2.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
45.0 °F - closed cup
flash_point_c
7.22 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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An expedient and multikilogram synthesis of a naphthalenoid H3 antagonist.
Pu YM, et al.
Organic Process Research & Development, 11(6), 1004-1009 (2007)
In vitro SAR of pyrrolidine-containing histamine H 3 receptor antagonists: Trends across multiple chemical series
Nersesian, Diana L., et al.
Bioorganic & Medicinal Chemistry Letters, 18.1, 355-359 (2008)
Optical Activation of Racemic a-Substituted Carbonyl Compounds Using Optically Active Amines.
Matsushita H, et al.
Bulletin of the Chemical Society of Japan, 49(7), 1928-1930 (1976)
Organic Process Research & Development, 11, 1004-1004 (2007)
Synthesis and structure?activity relationships of 4, 5-fused pyridazinones as histamine H 3 receptor antagonists
Tao, Ming, et al.
Bioorganic & Medicinal Chemistry Letters, 21.20, 6126-6130 (2011)
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