tert-Butyl 4-aminobenzylcarbamate hydrochloride

≥95%

Reagent Code: #118865
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CAS Number 174959-54-7

science Other reagents with same CAS 174959-54-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.74 g/mol
Formula C₁₂H₁₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD14584448
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals. It plays a role in the development of compounds with potential therapeutic applications, such as inhibitors or modulators of biological targets. Its structure is valuable in medicinal chemistry for designing and optimizing drug candidates. Additionally, it can be employed in peptide synthesis, where it serves as a protecting group for amines, ensuring selective reactions during complex molecule assembly. Its hydrochloride form enhances stability and solubility, making it suitable for various laboratory and industrial processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿657.00
inventory 1g
10-20 days ฿1,998.00
inventory 100mg
10-20 days ฿396.00

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tert-Butyl 4-aminobenzylcarbamate hydrochloride
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals. It plays a role in the development of compounds with potential therapeutic applications, such as inhibitors or modulators of biological targets. Its structure is valuable in medicinal chemistry for designing and optimizing drug candidates. Additionally, it can be employed in peptide synthesis, where it serves as a protecting group for amines, ensuring selective reactions during complex molecule assembly. Its

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals. It plays a role in the development of compounds with potential therapeutic applications, such as inhibitors or modulators of biological targets. Its structure is valuable in medicinal chemistry for designing and optimizing drug candidates. Additionally, it can be employed in peptide synthesis, where it serves as a protecting group for amines, ensuring selective reactions during complex molecule assembly. Its hydrochloride form enhances stability and solubility, making it suitable for various laboratory and industrial processes.

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