AA21189
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $116.00 | $81.00 | - + | |
250mg | 95% | in stock | $192.00 | $134.00 | - + | |
500mg | 95% | in stock | $319.00 | $224.00 | - + | |
1g | 95% | in stock | $479.00 | $335.00 | - + | |
5g | 95% | in stock | $1,435.00 | $1,004.00 | - + | |
10g | 95% | in stock | $2,391.00 | $1,674.00 | - + | |
25g | 95% | in stock | $4,781.00 | $3,347.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA21189 |
Chemical Name: | 2-Chloro-7-iodo-5h-pyrrolo[3,2-d]pyrimidine |
CAS Number: | 1152475-50-7 |
Molecular Formula: | C6H3ClIN3 |
Molecular Weight: | 279.46559 |
MDL Number: | MFCD12406130 |
SMILES: | Clc1ncc2c(n1)c(I)c[nH]2 |
Complexity: | 157 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 2 |
2-Chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the preparation of complex organic molecules and pharmaceutical intermediates. With its specific molecular structure, 2-Chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine exhibits remarkable potential in various synthetic applications, including the development of novel drug candidates, agrochemicals, and materials science. In the realm of medicinal chemistry, this compound plays a crucial role in the synthesis of potent bioactive compounds with diverse pharmacological activities. Its strategic incorporation into molecular frameworks allows for the enhancement of desired biological properties, making it an essential tool for drug discovery and development. Furthermore, in the field of organic synthesis, 2-Chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine serves as a key intermediate in the construction of intricate molecular architectures, enabling chemists to access a wide array of structurally complex compounds efficiently. Its reactivity and compatibility with various coupling reactions make it a valuable resource for synthetic chemists aiming to streamline multi-step syntheses and achieve high levels of molecular complexity.