tert-Butyl S-2-pyrrolidone-5-carboxylate

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Reagent Code: #143337
label
Alias L-pyroglutamate tert-butyl ester
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CAS Number 35418-16-7

science Other reagents with same CAS 35418-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.22 g/mol
Formula C₉H₁₅NO₃
badge Registry Numbers
EC Number 252-555-5
MDL Number MFCD06659481
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

tert-Butyl (S)-2-pyrrolidone-5-carboxylate is a chiral building block and key intermediate in organic synthesis, particularly for pharmaceutical applications. As the tert-butyl ester of L-pyroglutamic acid, it enables stereoselective reactions essential for producing optically active compounds. It is widely used in the synthesis of nootropic drugs, such as piracetam and other racetams, where it improves reaction yields and enantioselectivity. In peptide synthesis, it acts as a protected pyroglutamic acid derivative, offering stability during synthesis and facile deprotection of the ester group under acidic conditions to yield the free carboxylic acid.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿137.50
inventory 5g
10-20 days ฿165.00
inventory 25g
10-20 days ฿930.00
inventory 100g
10-20 days ฿3,120.00
inventory 500g
10-20 days ฿15,260.00

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tert-Butyl S-2-pyrrolidone-5-carboxylate
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tert-Butyl (S)-2-pyrrolidone-5-carboxylate is a chiral building block and key intermediate in organic synthesis, particularly for pharmaceutical applications. As the tert-butyl ester of L-pyroglutamic acid, it enables stereoselective reactions essential for producing optically active compounds. It is widely used in the synthesis of nootropic drugs, such as piracetam and other racetams, where it improves reaction yields and enantioselectivity. In peptide synthesis, it acts as a protected pyroglutamic acid

tert-Butyl (S)-2-pyrrolidone-5-carboxylate is a chiral building block and key intermediate in organic synthesis, particularly for pharmaceutical applications. As the tert-butyl ester of L-pyroglutamic acid, it enables stereoselective reactions essential for producing optically active compounds. It is widely used in the synthesis of nootropic drugs, such as piracetam and other racetams, where it improves reaction yields and enantioselectivity. In peptide synthesis, it acts as a protected pyroglutamic acid derivative, offering stability during synthesis and facile deprotection of the ester group under acidic conditions to yield the free carboxylic acid.

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