1020056-56-7 | 4-Chloro-5-methyl-1h-pyrrolo[2,3-b]pyridine

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$32.00	$23.00
250mg	98%	in stock	$53.00	$38.00
1g	98%	in stock	$139.00	$98.00

Description

• Catalog Number: AA07958
• Chemical Name: 4-Chloro-5-methyl-1h-pyrrolo[2,3-b]pyridine
• CAS Number: 1020056-56-7
• Molecular Formula: C8H7ClN2
• Molecular Weight: 166.6076
• MDL Number: MFCD09965882
• SMILES: Cc1cnc2c(c1Cl)cc[nH]2

Computed Properties

• Complexity: 151
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.3

Upstream Synthesis Route

4-Chloro-5-methyl-1H-pyrrolo[2,3-b]pyridine is a versatile compound commonly used in chemical synthesis for various applications. This heterocyclic compound with a chloro and methyl group attached to the five-membered pyrrole ring offers a range of reactivity that makes it valuable in organic chemistry. In particular, it serves as a crucial building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.One important application of 4-Chloro-5-methyl-1H-pyrrolo[2,3-b]pyridine is its role as a key intermediate in the synthesis of biologically active compounds. Its unique structural features allow for selective functionalization, enabling chemists to introduce specific substituents that can modulate the compound's biological activity. This compound has found use in the development of potential drug candidates for various therapeutic targets, including anticancer agents, antimicrobial compounds, and enzyme inhibitors.Furthermore, 4-Chloro-5-methyl-1H-pyrrolo[2,3-b]pyridine is utilized in the synthesis of functional materials with specific properties. By incorporating this compound into organic frameworks, researchers can tailor the material's electronic, optical, or magnetic characteristics for applications in sensors, optoelectronic devices, or molecular electronics. Its presence in the molecular structure can impart desired properties such as fluorescence, conductivity, or chirality, making it an essential component in the design of advanced materials.Overall, the versatility and reactivity of 4-Chloro-5-methyl-1H-pyrrolo[2,3-b]pyridine make it a valuable tool in the hands of synthetic chemists seeking to access complex molecular architectures for various purposes in drug discovery, materials science, and chemical research.