refractive index
n20/D 1.4353
Quality Level
density
0.842 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C[C@@H]1CCCN1
InChI
1S/C5H11N/c1-5-3-2-4-6-5/h5-6H,2-4H2,1H3/t5-/m1/s1
InChI key
RGHPCLZJAFCTIK-RXMQYKEDSA-N
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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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Certificates of Analysis (COA)
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Find documentation for the products that you have recently purchased in the Document Library.
An expedient and multikilogram synthesis of a naphthalenoid H3 antagonist.
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
Bioorganic & Medicinal Chemistry Letters, 18.1, 355-359 (2008)
Optical Activation of Racemic a-Substituted Carbonyl Compounds Using Optically Active Amines.
Bulletin of the Chemical Society of Japan, 49(7), 1928-1930 (1976)
A new class of potent non-imidazole H 3 antagonists: 2-aminoethylbenzofurans
Bioorganic & Medicinal Chemistry Letters, 14.3, 689-693 (2004)
Organic Process Research & Development, 11, 1004-1004 (2007)
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