1008-07-7 | 7-Chloro-3-formylindole

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$18.00	$13.00
250mg	97%	in stock	$33.00	$23.00
1g	97%	in stock	$81.00	$57.00
5g	97%	in stock	$322.00	$225.00
25g	97%	in stock	$1,224.00	$857.00

Description

• Catalog Number: AA03571
• Chemical Name: 7-Chloro-3-formylindole
• CAS Number: 1008-07-7
• Molecular Formula: C9H6ClNO
• Molecular Weight: 179.603
• MDL Number: MFCD06657153
• SMILES: O=Cc1c[nH]c2c1cccc2Cl

Computed Properties

• Complexity: 185
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.1

Upstream Synthesis Route

7-Chloro-1H-indole-3-carbaldehyde is a versatile chemical compound used in a wide range of chemical synthesis applications. This compound is commonly employed as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique chemical structure and reactivity make it an important intermediate for the production of complex organic molecules.In organic synthesis, 7-Chloro-1H-indole-3-carbaldehyde serves as a valuable starting material for the preparation of indole derivatives, which are widely found in natural products and biologically active compounds. By undergoing various chemical reactions such as condensation, reduction, and cyclization, this compound can be transformed into a diverse array of indole-based molecules with potential pharmaceutical or industrial applications.Additionally, 7-Chloro-1H-indole-3-carbaldehyde can participate in multi-step synthesis routes to produce heterocyclic compounds, which are crucial components in medicinal chemistry and material science. Its ability to function as a versatile synthon allows chemists to access structurally complex molecules efficiently and selectively, enabling the development of novel drugs, catalysts, and functional materials.Overall, the strategic use of 7-Chloro-1H-indole-3-carbaldehyde in chemical synthesis showcases its significance as a valuable building block for creating diverse and intricate organic molecules with promising properties and applications in various fields.

Literature

• Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury.

  Nature chemical biology 20050701