6-Acetonyl-N-methyl-dihydrodecarine

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Reagent Code: #136801
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CAS Number 1253740-09-8

science Other reagents with same CAS 1253740-09-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.42 g/mol
Formula C₂₃H₂₁NO₅
badge Registry Numbers
MDL Number MFCD20274578
inventory_2 Storage & Handling
Storage 2-8℃, dry, closed

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. Shows potential in the development of agents targeting neurological pathways due to its structural affinity with neuroactive alkaloids. Investigated for its role in modulating cellular signaling, particularly in studies related to pain perception and central nervous system activity. Also explored for anti-inflammatory properties in preclinical models. Its lipophilic nature allows for better membrane permeability, making it suitable for studies requiring blood-brain barrier penetration.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿30,010.00

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6-Acetonyl-N-methyl-dihydrodecarine
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Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. Shows potential in the development of agents targeting neurological pathways due to its structural affinity with neuroactive alkaloids. Investigated for its role in modulating cellular signaling, particularly in studies related to pain perception and central nervous system activity. Also explored for anti-inflammatory properties in preclinical models. Its lipophilic nature allows for better membrane perm

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. Shows potential in the development of agents targeting neurological pathways due to its structural affinity with neuroactive alkaloids. Investigated for its role in modulating cellular signaling, particularly in studies related to pain perception and central nervous system activity. Also explored for anti-inflammatory properties in preclinical models. Its lipophilic nature allows for better membrane permeability, making it suitable for studies requiring blood-brain barrier penetration.

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