30515-28-7 | 7-Bromoheptanoic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$10.00	$7.00
10g	98%	in stock	$15.00	$10.00
25g	98%	in stock	$28.00	$19.00

Description

• Catalog Number: AB40305
• Chemical Name: 7-Bromoheptanoic acid
• CAS Number: 30515-28-7
• Molecular Formula: C7H13BrO2
• Molecular Weight: 209.0809
• MDL Number: MFCD00037800
• SMILES: BrCCCCCCC(=O)O

Computed Properties

• Complexity: 93.6
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 6
• XLogP3: 1

Upstream Synthesis Route

7-Bromoheptanoic acid is a versatile compound commonly utilized in organic synthesis as a key intermediate for various chemical reactions. Its unique structure, with a bromine functional group on the seventh carbon atom of a heptanoic acid chain, lends itself to a wide range of applications in the field of chemistry.In chemical synthesis, 7-Bromoheptanoic acid serves as a valuable building block for the creation of diverse organic molecules. Its bromine group can undergo substitution reactions with nucleophiles to introduce new functional groups or modify existing ones. This ability makes it particularly useful in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.Furthermore, 7-Bromoheptanoic acid can participate in various coupling reactions, such as esterification, amidation, and Heck coupling, to form complex molecular structures. These reactions enable chemists to access a diverse array of compounds for research, development, and industrial applications.Overall, the application of 7-Bromoheptanoic acid in chemical synthesis exemplifies its importance as a versatile and indispensable tool for creating novel molecules with tailored properties and functionalities.

Literature

• Enantioselective synthesis of pentacycloanammoxic acid.

  Journal of the American Chemical Society 20060315

• Total synthesis of (+/-)-pentacycloanammoxic acid.

  Journal of the American Chemical Society 20041208