137628-17-2 | 2,3-Dibromo-5-chloropyridine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$8.00	$5.00
5g	95%	in stock	$9.00	$6.00
10g	95%	in stock	$15.00	$10.00
25g	95%	in stock	$16.00	$12.00
250g	95%	in stock	$152.00	$106.00

Description

• Catalog Number: AA51210
• Chemical Name: 2,3-Dibromo-5-chloropyridine
• CAS Number: 137628-17-2
• Molecular Formula: C5H2Br2ClN
• Molecular Weight: 271.3371
• MDL Number: MFCD08687254
• SMILES: Clc1cnc(c(c1)Br)Br

Computed Properties

• Complexity: 101
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 3.2

Upstream Synthesis Route

2,3-Dibromo-5-chloropyridine is a versatile compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the development of various organic molecules due to its unique structure and reactivity. Its application in the synthesis of pharmaceuticals, agrochemicals, and materials has been well-documented in the scientific literature.In organic synthesis, 2,3-Dibromo-5-chloropyridine can act as a halogenated scaffold that can undergo diverse functionalization reactions such as nucleophilic substitution, cross-coupling, and metal-catalyzed transformations. These chemical reactions enable the modification of the pyridine ring to introduce different functionalities or create complex molecular structures.One key application of 2,3-Dibromo-5-chloropyridine is its utility in the preparation of biologically active compounds. By incorporating this building block into drug molecules, researchers can manipulate the pharmacological properties of the final compounds, leading to the development of new therapeutic agents. Additionally, the presence of bromine and chlorine atoms in the pyridine ring can impart specific physicochemical properties to the synthesized products, making them suitable for targeted applications.Furthermore, 2,3-Dibromo-5-chloropyridine is employed in the synthesis of advanced materials such as liquid crystals, polymers, and dyes. Its ability to participate in polymerization reactions or form coordination complexes with metal ions makes it a valuable tool for designing functional materials with tailored properties.Overall, the strategic use of 2,3-Dibromo-5-chloropyridine in chemical synthesis enables chemists to access a wide range of molecular scaffolds with diverse functionalities, paving the way for the discovery of novel compounds with potential applications in various industries.