4-CHLORO-5-IODO-7-METHYL-7H-PYRROLO[2,3-D]PYRIMIDINE

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Reagent Code: #47172
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CAS Number 833481-37-1

science Other reagents with same CAS 833481-37-1

blur_circular Chemical Specifications

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Weight 293.49 g/mol
Formula C₇H₅ClIN₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting kinase enzymes. Its structure makes it valuable for developing inhibitors that can modulate signaling pathways involved in diseases such as cancer and inflammatory disorders. Additionally, it is employed in the design of nucleoside analogs, which are critical in antiviral and anticancer drug development. Its halogenated pyrrolopyrimidine core is often modified to enhance binding affinity and selectivity for specific therapeutic targets.

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inventory 1g
10-20 days ฿32,733.00

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4-CHLORO-5-IODO-7-METHYL-7H-PYRROLO[2,3-D]PYRIMIDINE
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting kinase enzymes. Its structure makes it valuable for developing inhibitors that can modulate signaling pathways involved in diseases such as cancer and inflammatory disorders. Additionally, it is employed in the design of nucleoside analogs, which are critical in antiviral and anticancer

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting kinase enzymes. Its structure makes it valuable for developing inhibitors that can modulate signaling pathways involved in diseases such as cancer and inflammatory disorders. Additionally, it is employed in the design of nucleoside analogs, which are critical in antiviral and anticancer drug development. Its halogenated pyrrolopyrimidine core is often modified to enhance binding affinity and selectivity for specific therapeutic targets.

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