(R)-2-(tert-Butoxycarbonyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid

98%

Reagent Code: #229344
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CAS Number 2703746-30-7

science Other reagents with same CAS 2703746-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.34 g/mol
Formula C₁₆H₂₁NO₅
badge Registry Numbers
MDL Number MFCD34165732
thermostat Physical Properties
Boiling Point 475.4±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.225±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting neurological and cardiovascular diseases. Its structure supports the construction of complex alkaloids and enzyme inhibitors. The tert-butoxycarbonyl (Boc) group allows for selective protection of amines during peptide coupling and multistep syntheses. Commonly employed in asymmetric synthesis due to the stereogenic center, enabling high enantioselectivity in drug candidates. Also utilized in the preparation of protease inhibitors and receptor agonists/antagonists where precise spatial orientation of functional groups is critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,110.00
inventory 250mg
10-20 days ฿39,140.00
inventory 1g
10-20 days ฿97,700.00

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(R)-2-(tert-Butoxycarbonyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting neurological and cardiovascular diseases. Its structure supports the construction of complex alkaloids and enzyme inhibitors. The tert-butoxycarbonyl (Boc) group allows for selective protection of amines during peptide coupling and multistep syntheses. Commonly employed in asymmetric synthesis due to the stereogenic center, enabling high enantioselectivity in drug candidates. Also utilized in the preparation of protease inhibitors and receptor agonists/antagonists where precise spatial orientation of functional groups is critical.
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