4-Amino-1-methyl-1H-imidazole-2-carboxamide

90%

Reagent Code: #138664
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CAS Number 827588-62-5

science Other reagents with same CAS 827588-62-5

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inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and participate in heterocyclic ring systems, enhancing binding affinity to biological targets. Also employed in the preparation of antiviral agents and enzyme modulators. Its structural features make it valuable in optimizing drug potency and selectivity during lead compound development.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿8,420.00
50mg
10-20 days ฿11,790.00
100mg
10-20 days ฿16,480.00
250mg
10-20 days ฿24,710.00
1g
10-20 days ฿75,830.00

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4-Amino-1-methyl-1H-imidazole-2-carboxamide
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and participate in heterocyclic ring systems, enhancing binding affinity to biological targets. Also employed in the preparation of antiviral agents and enzyme modulators. Its structural features make it valuable in optimizing drug potency and selectivity during lead c
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and participate in heterocyclic ring systems, enhancing binding affinity to biological targets. Also employed in the preparation of antiviral agents and enzyme modulators. Its structural features make it valuable in optimizing drug potency and selectivity during lead compound development.
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