Benzyl2,5-diazabicyclo[4.1.0]Heptane-2-carboxylatehydrochloride

98%

Reagent Code: #155978
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CAS Number 2387602-63-1

science Other reagents with same CAS 2387602-63-1

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scatter_plot Molecular Information
Weight 268.74 g/mol
Formula C₁₃H₁₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD32670458
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a pharmaceutical intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for mimicking peptide conformations and enhancing metabolic stability in drug candidates. It is also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, contributing to the production of enantiomerically pure drugs. The hydrochloride salt form improves solubility and handling in aqueous and polar organic solvents during synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,380.00
inventory 250mg
10-20 days ฿18,580.00
inventory 500mg
10-20 days ฿32,490.00
inventory 1g
10-20 days ฿55,850.00

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Benzyl2,5-diazabicyclo[4.1.0]Heptane-2-carboxylatehydrochloride
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Used primarily as a pharmaceutical intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for mimicking peptide conformations and enhancing metabolic stability in drug candidates. It is also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, contributing to the production of enantiomerically pure drugs. The hydrochloride salt f

Used primarily as a pharmaceutical intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for mimicking peptide conformations and enhancing metabolic stability in drug candidates. It is also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, contributing to the production of enantiomerically pure drugs. The hydrochloride salt form improves solubility and handling in aqueous and polar organic solvents during synthetic processes.

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