N-((1R,2S)-1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-1-hydroxy-3-(pyrrolidin-1-yl)propan-2-yl)octanamide

95%

Reagent Code: #215061
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CAS Number 1092472-65-5

science Other reagents with same CAS 1092472-65-5

blur_circular Chemical Specifications

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Weight 404.54 g/mol
Formula C₂₃H₃₆N₂O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of beta-adrenergic receptor modulators. It plays a role in developing compounds targeting cardiovascular and pulmonary diseases due to its structural affinity for adrenergic pathways. Its lipophilic side chain enhances membrane permeability, improving bioavailability in drug formulations. Also investigated for potential use in central nervous system agents owing to its ability to cross the blood-brain barrier. Currently in laboratory-stage biological evaluation and not yet used commercially.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿432,000.00

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N-((1R,2S)-1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-1-hydroxy-3-(pyrrolidin-1-yl)propan-2-yl)octanamide
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Used in pharmaceutical research as a key intermediate in the synthesis of beta-adrenergic receptor modulators. It plays a role in developing compounds targeting cardiovascular and pulmonary diseases due to its structural affinity for adrenergic pathways. Its lipophilic side chain enhances membrane permeability, improving bioavailability in drug formulations. Also investigated for potential use in central nervous system agents owing to its ability to cross the blood-brain barrier. Currently in laboratory-

Used in pharmaceutical research as a key intermediate in the synthesis of beta-adrenergic receptor modulators. It plays a role in developing compounds targeting cardiovascular and pulmonary diseases due to its structural affinity for adrenergic pathways. Its lipophilic side chain enhances membrane permeability, improving bioavailability in drug formulations. Also investigated for potential use in central nervous system agents owing to its ability to cross the blood-brain barrier. Currently in laboratory-stage biological evaluation and not yet used commercially.

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