875781-44-5 | 2-Bromo-7-iodo-5H-pyrrolo[2,3-b]pyrazine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$40.00	$28.00
5g	95%	in stock	$101.00	$71.00
25g	95%	in stock	$415.00	$291.00
50g	95%	in stock	$623.00	$436.00
100g	95%	in stock	$1,037.00	$726.00

Description

• Catalog Number: AB61483
• Chemical Name: 2-Bromo-7-iodo-5H-pyrrolo[2,3-b]pyrazine
• CAS Number: 875781-44-5
• Molecular Formula: C6H3BrIN3
• Molecular Weight: 323.9165899999999
• MDL Number: MFCD09878696
• SMILES: Brc1cnc2c(n1)c(I)c[nH]2

Computed Properties

• Complexity: 157
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 2

Upstream Synthesis Route

5-Bromo-3-iodo-4,7-diazaindole is a versatile building block in chemical synthesis, commonly utilized in the pharmaceutical and agrochemical industries. This compound serves as a valuable intermediate in the formation of complex organic molecules due to its unique structural properties. In chemical synthesis, 5-Bromo-3-iodo-4,7-diazaindole can be employed as a key starting material for the construction of biologically active compounds, such as potential drug candidates or crop protection agents. Its strategic positioning of bromine and iodine atoms within a diazaindole scaffold allows for selective functionalization at specific sites, enabling the creation of diverse chemical libraries for screening purposes.Furthermore, the presence of bromine and iodine atoms in 5-Bromo-3-iodo-4,7-diazaindole imparts reactivity and compatibility with various coupling reactions, including cross-coupling reactions and transition metal-catalyzed transformations. This reactivity profile makes it an attractive substrate for the synthesis of heterocyclic compounds with enhanced biological activities.Overall, the application of 5-Bromo-3-iodo-4,7-diazaindole in chemical synthesis offers a pathway to access structurally diverse and pharmacologically relevant molecules, making it a valuable tool for medicinal and agricultural chemistry research.