1086376-43-3 | 5-Bromo-4,6-dichloro-2-methylpyrimidine

Packsize	Purity	Availability	Price	Discounted Price
1mg		2 weeks	$105.00	$73.00
2mg		2 weeks	$123.00	$86.00
3mg		2 weeks	$149.00	$105.00
5mg		2 weeks	$168.00	$118.00
10mg		2 weeks	$193.00	$135.00
100mg		2 weeks	$1,067.00	$747.00
250mg		2 weeks	$1,392.00	$975.00
1g		2 weeks	$2,562.00	$1,794.00

Description

• Catalog Number: AE31719
• Chemical Name: 5-Bromo-4,6-dichloro-2-methylpyrimidine
• CAS Number: 1086376-43-3
• Molecular Formula: C5H3BrCl2N2
• Molecular Weight: 241.9007
• MDL Number: MFCD09864954
• SMILES: Cc1nc(Cl)c(c(n1)Cl)Br

Computed Properties

• Complexity: 112
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 3.2

Upstream Synthesis Route

The 5-Bromo-4,6-dichloro-2-methylpyrimidine is a versatile compound that finds wide application in chemical synthesis processes. This unique compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its specific chemical properties make it a crucial intermediate in the preparation of complex organic molecules.In chemical synthesis, 5-Bromo-4,6-dichloro-2-methylpyrimidine acts as a key reagent in the formation of heterocyclic structures. Its reactive nature allows for selective functionalization, enabling the introduction of specific substituents at desired positions within a molecule. This control over regioselectivity and reactivity is essential for the successful synthesis of target compounds with high efficiency and accuracy.Moreover, the incorporation of 5-Bromo-4,6-dichloro-2-methylpyrimidine into synthetic pathways facilitates the construction of molecules with diverse properties and functions. Its ability to participate in various chemical reactions, such as nucleophilic substitutions and palladium-catalyzed cross-coupling reactions, broadens its utility in creating novel molecular architectures.Overall, the strategic inclusion of 5-Bromo-4,6-dichloro-2-methylpyrimidine in chemical synthesis processes enables chemists to access a wide range of structurally complex and biologically active compounds, making it a valuable tool in the development of advanced materials and pharmaceutical agents.