(S)-()-2-(Aminomethyl)pyrrolidine

97%

Reagent Code: #234221
label
Alias S-2-aminomethylpyrrolidine(S)-(+)-2-(aminomethyl)pyrrolidine
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CAS Number 69500-64-7

science Other reagents with same CAS 69500-64-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 100.16 g/mol
Formula C₅H₁₂N₂
badge Registry Numbers
MDL Number MFCD00191745
thermostat Physical Properties
Boiling Point 65 °C11 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.933 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its primary amine and secondary amine groups allow for versatile functionalization, making it valuable in the preparation of enzyme inhibitors, receptor agonists, and antagonists. Commonly employed in the manufacture of central nervous system (CNS) agents and cardiovascular drugs. Also utilized in asymmetric synthesis and catalysis due to its chiral structure.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,900.00
inventory 500mg
10-20 days ฿27,760.00
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(S)-()-2-(Aminomethyl)pyrrolidine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its primary amine and secondary amine groups allow for versatile functionalization, making it valuable in the preparation of enzyme inhibitors, receptor agonists, and antagonists. Commonly employed in the manufacture of central nervous system (CNS) agents and cardiovascular drugs. Also utilized

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its primary amine and secondary amine groups allow for versatile functionalization, making it valuable in the preparation of enzyme inhibitors, receptor agonists, and antagonists. Commonly employed in the manufacture of central nervous system (CNS) agents and cardiovascular drugs. Also utilized in asymmetric synthesis and catalysis due to its chiral structure.

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