(R)-(-)-2-Methylpyrrolidine

95%

Reagent Code: #229875
label
Alias (R)-2-methylpyrrolidine (R)-2-methylpyrrolidine
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CAS Number 41720-98-3

science Other reagents with same CAS 41720-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 85.15000000000001 g/mol
Formula C₅H₁₁N
badge Registry Numbers
MDL Number MFCD07783026
inventory_2 Storage & Handling
Density 0.842
Storage Room temperature, flammable area

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its stereochemistry makes it valuable in asymmetric synthesis, particularly in the development of drugs requiring specific enantiomeric forms. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-enantiomer contributes to desired biological activity. Also utilized as a reagent or intermediate in agrochemicals and specialty chemicals requiring enantiopure amines. Its cyclic secondary amine structure allows for use in catalysis and organocatalytic reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿600.00
1g
10-20 days ฿1,850.00
5g
10-20 days ฿9,190.00
(R)-(-)-2-Methylpyrrolidine
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Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its stereochemistry makes it valuable in asymmetric synthesis, particularly in the development of drugs requiring specific enantiomeric forms. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-enantiomer contributes to desired biological activity. Also utilized as a reagent or intermediate in agrochemicals and specialty chemicals requiring enantiopure amines.

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its stereochemistry makes it valuable in asymmetric synthesis, particularly in the development of drugs requiring specific enantiomeric forms. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-enantiomer contributes to desired biological activity. Also utilized as a reagent or intermediate in agrochemicals and specialty chemicals requiring enantiopure amines. Its cyclic secondary amine structure allows for use in catalysis and organocatalytic reactions.

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