6-(Bromomethyl)pteridine-2,4-diamine hydrobromide
90%
- Product Code: 72607
CAS:
52853-40-4
Molecular Weight: | 335.99 g./mol | Molecular Formula: | C₇H₈Br₂N₆ |
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EC Number: | MDL Number: | ||
Melting Point: | >195°C | Boiling Point: | |
Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of various pharmaceutical agents, particularly those targeting enzyme inhibition. Its structure is valuable for modifying pteridine derivatives, which are often explored for their potential in treating diseases such as cancer, bacterial infections, and inflammatory conditions. Additionally, it is employed in research to study the biochemical pathways involving folate metabolism, as pteridine derivatives play a significant role in these processes. The bromomethyl group in the compound allows for further functionalization, making it a versatile building block in the synthesis of complex molecules.
Product Specification:
Test | Specification |
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APPEARANCE | Light Brown to Brown Solid |
PURITY | 89.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $36.55 |
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1.000 | 10-20 days | $74.34 |
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5.000 | 10-20 days | $239.21 |
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25.000 | 10-20 days | $715.13 |
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100.000 | 10-20 days | $2,167.81 |
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6-(Bromomethyl)pteridine-2,4-diamine hydrobromide
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of various pharmaceutical agents, particularly those targeting enzyme inhibition. Its structure is valuable for modifying pteridine derivatives, which are often explored for their potential in treating diseases such as cancer, bacterial infections, and inflammatory conditions. Additionally, it is employed in research to study the biochemical pathways involving folate metabolism, as pteridine derivatives play a significant role in these processes. The bromomethyl group in the compound allows for further functionalization, making it a versatile building block in the synthesis of complex molecules.
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