rel-(3R,4R)-N3,N3-Dimethyltetrahydrofuran-3,4-diamine

97%

Reagent Code: #231993
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CAS Number 728008-13-7

science Other reagents with same CAS 728008-13-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.19 g/mol
Formula C₆H₁₄N₂O
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its rigid tetrahydrofuran backbone and defined stereochemistry make it valuable in asymmetric synthesis and as a scaffold in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemical control is critical. Also utilized in agrochemicals for the creation of enantioselective herbicides and pesticides. Its amine functionality allows for easy derivatization, enabling rapid exploration of structure-activity relationships in drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,550.00
rel-(3R,4R)-N3,N3-Dimethyltetrahydrofuran-3,4-diamine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its rigid tetrahydrofuran backbone and defined stereochemistry make it valuable in asymmetric synthesis and as a scaffold in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemical control is critical. Also utilized in agrochemicals for the creation of en
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its rigid tetrahydrofuran backbone and defined stereochemistry make it valuable in asymmetric synthesis and as a scaffold in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemical control is critical. Also utilized in agrochemicals for the creation of enantioselective herbicides and pesticides. Its amine functionality allows for easy derivatization, enabling rapid exploration of structure-activity relationships in drug discovery.
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