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Structure of 1445-08-5
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2-Methyl-6-aminopurine delivers a purine scaffold with enhanced solubility and stability, enabling direct incorporation into nucleoside analogs and oligonucleotide synthesis. This bench-stable derivative features a primary amine at the 6-position and a methyl group at the 2-position, facilitating selective functionalization in medicinal chemistry and biochemical studies.
2-Methyl-6-aminopurine serves as a key purine scaffold for medicinal chemistry and nucleoside analog synthesis. Its amino group at C6 enables straightforward derivatization, while the methyl substitution at C2 enhances metabolic stability and modulates hydrogen-bonding capacity. The compound exhibits bench-stable handling, tolerates diverse reaction conditions, and functions as a reliable building block in the construction of antiviral and anticancer agents.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: