tert-butyl 4-bromo-1H-imidazole-1-carboxylate-2,5-d2

95%

Reagent Code: #54305
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CAS Number 1622844-09-0

science Other reagents with same CAS 1622844-09-0

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inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of deuterated compounds, which are valuable in drug discovery and development due to their enhanced metabolic stability and pharmacokinetic properties. The deuterium labeling (2,5-d2) in the imidazole ring is particularly useful in mechanistic studies and tracing metabolic pathways. The 4-bromo substituent provides a reactive handle for further functionalization, such as through cross-coupling or substitution reactions, allowing the construction of diverse imidazole-based libraries. Additionally, it is employed in the synthesis of biologically active molecules, such as inhibitors or ligands, targeting specific enzymes or receptors. Its tert-butyl and carboxylate groups provide steric and electronic protection, facilitating selective reactions in complex synthetic routes.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿8,220.00
inventory 5mg
10-20 days ฿28,880.00

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tert-butyl 4-bromo-1H-imidazole-1-carboxylate-2,5-d2
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This chemical is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of deuterated compounds, which are valuable in drug discovery and development due to their enhanced metabolic stability and pharmacokinetic properties. The deuterium labeling (2,5-d2) in the imidazole ring is particularly useful in mechanistic studies and tracing metabolic pathways. The 4-bromo substituent provides a reactive handle for further functionalization,

This chemical is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of deuterated compounds, which are valuable in drug discovery and development due to their enhanced metabolic stability and pharmacokinetic properties. The deuterium labeling (2,5-d2) in the imidazole ring is particularly useful in mechanistic studies and tracing metabolic pathways. The 4-bromo substituent provides a reactive handle for further functionalization, such as through cross-coupling or substitution reactions, allowing the construction of diverse imidazole-based libraries. Additionally, it is employed in the synthesis of biologically active molecules, such as inhibitors or ligands, targeting specific enzymes or receptors. Its tert-butyl and carboxylate groups provide steric and electronic protection, facilitating selective reactions in complex synthetic routes.

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