tert-Butyl 3-cyano-3-methylpyrrolidine-1-carboxylate

98%

Reagent Code: #150598
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CAS Number 1228537-69-6

science Other reagents with same CAS 1228537-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.27 g/mol
Formula C₁₁H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD26406713
thermostat Physical Properties
Boiling Point 310.2±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. This compound features a pyrrolidine ring substituted with cyano and methyl groups at the 3-position, and a tert-butyl carbamate (Boc) protecting group on the nitrogen. Its nitrile and pyrrolidine functionalities make it valuable for constructing complex nitrogen-containing compounds. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in the design of enzyme inhibitors and receptor modulators. The Boc group allows for easy protection of the nitrogen, enabling selective reactions at other sites, such as hydrolysis or reduction of the nitrile, during multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,750.00
inventory 1g
10-20 days ฿6,980.00

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tert-Butyl 3-cyano-3-methylpyrrolidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. This compound features a pyrrolidine ring substituted with cyano and methyl groups at the 3-position, and a tert-butyl carbamate (Boc) protecting group on the nitrogen. Its nitrile and pyrrolidine functionalities make it valuable for constructing complex nitrogen-containing compounds. Commonly employed in medicinal chemistry for structure-activity relationship studies, especial

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. This compound features a pyrrolidine ring substituted with cyano and methyl groups at the 3-position, and a tert-butyl carbamate (Boc) protecting group on the nitrogen. Its nitrile and pyrrolidine functionalities make it valuable for constructing complex nitrogen-containing compounds. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in the design of enzyme inhibitors and receptor modulators. The Boc group allows for easy protection of the nitrogen, enabling selective reactions at other sites, such as hydrolysis or reduction of the nitrile, during multi-step syntheses.

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