tert-butyl (3R,4R)-3,4-dihydroxypyrrolidine-1-carboxylate

98%

Reagent Code: #231500
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CAS Number 150986-62-2

science Other reagents with same CAS 150986-62-2

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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antiviral and antidiabetic agents. Its diol structure with N-Boc protection and defined stereochemistry makes it valuable for constructing complex molecules where stereocontrol is critical. Commonly employed in asymmetric synthesis to introduce the pyrrolidine scaffold while preserving the (3R,4R) configuration. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection of the nitrogen during multi-step syntheses, enhancing its utility in medicinal chemistry and process development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,730.00
inventory 250mg
10-20 days ฿6,220.00
inventory 1g
10-20 days ฿15,570.00

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tert-butyl (3R,4R)-3,4-dihydroxypyrrolidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antiviral and antidiabetic agents. Its diol structure with N-Boc protection and defined stereochemistry makes it valuable for constructing complex molecules where stereocontrol is critical. Commonly employed in asymmetric synthesis to introduce the pyrrolidine scaffold while preserving the (3R,4R) configuration. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection of the ni

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antiviral and antidiabetic agents. Its diol structure with N-Boc protection and defined stereochemistry makes it valuable for constructing complex molecules where stereocontrol is critical. Commonly employed in asymmetric synthesis to introduce the pyrrolidine scaffold while preserving the (3R,4R) configuration. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection of the nitrogen during multi-step syntheses, enhancing its utility in medicinal chemistry and process development.

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