(3R,4R)-rel-1-Benzyl-N,4-dimethylpiperidin-3-amine dihydrochloride

97%

Reagent Code: #230812
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CAS Number 477600-68-3

science Other reagents with same CAS 477600-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.26 g/mol
Formula C₁₄H₂₄Cl₂N₂
badge Registry Numbers
MDL Number MFCD11044501
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as analgesics and neuromodulators. Its stereochemistry makes it valuable in creating selective drug candidates targeting opioid receptors. Commonly employed in research settings for structure-activity relationship studies due to its rigid piperidine scaffold and functional group arrangement. Also utilized in the preparation of chiral ligands for asymmetric synthesis in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿370.00
5g
10-20 days ฿1,620.00
25g
10-20 days ฿4,818.00
(3R,4R)-rel-1-Benzyl-N,4-dimethylpiperidin-3-amine dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as analgesics and neuromodulators. Its stereochemistry makes it valuable in creating selective drug candidates targeting opioid receptors. Commonly employed in research settings for structure-activity relationship studies due to its rigid piperidine scaffold and functional group arrangement. Also utilized in the preparation of chiral ligands for asymmetric synthesis in medicinal

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as analgesics and neuromodulators. Its stereochemistry makes it valuable in creating selective drug candidates targeting opioid receptors. Commonly employed in research settings for structure-activity relationship studies due to its rigid piperidine scaffold and functional group arrangement. Also utilized in the preparation of chiral ligands for asymmetric synthesis in medicinal chemistry.

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