rel-(4aR,7aS)-Octahydrocyclopenta[b][1,4]oxazinehydrochloride

98%

Reagent Code: #232025
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CAS Number 1807941-05-4

science Other reagents with same CAS 1807941-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.65 g/mol
Formula C₇H₁₄ClNO
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MDL Number MFCD28145358
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural framework supports the creation of bioactive molecules with potential anxiolytic or antidepressant effects. The compound's rigid, polycyclic structure makes it valuable in medicinal chemistry for exploring structure-activity relationships in drug design. It is also employed in asymmetric synthesis due to its chiral centers, aiding in the production of enantiomerically pure compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,060.00
inventory 250mg
10-20 days ฿14,500.00
inventory 500mg
10-20 days ฿25,850.00
inventory 1g
10-20 days ฿41,320.00
rel-(4aR,7aS)-Octahydrocyclopenta[b][1,4]oxazinehydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural framework supports the creation of bioactive molecules with potential anxiolytic or antidepressant effects. The compound's rigid, polycyclic structure makes it valuable in medicinal chemistry for exploring structure-activity relationships in drug design. It is also employed in asymmetric synthesis due to its chiral centers, aiding in the production of enantiomerica

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structural framework supports the creation of bioactive molecules with potential anxiolytic or antidepressant effects. The compound's rigid, polycyclic structure makes it valuable in medicinal chemistry for exploring structure-activity relationships in drug design. It is also employed in asymmetric synthesis due to its chiral centers, aiding in the production of enantiomerically pure compounds.

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