1714-29-0 | 1-Bromopyrene

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$7.00	$5.00
10g	98%	in stock	$13.00	$10.00
25g	98%	in stock	$24.00	$17.00
100g	98%	in stock	$90.00	$63.00
500g	98%	in stock	$449.00	$315.00

Description

• Catalog Number: AB43309
• Chemical Name: 1-Bromopyrene
• CAS Number: 1714-29-0
• Molecular Formula: C16H9Br
• Molecular Weight: 281.1467
• MDL Number: MFCD00015767
• SMILES: Brc1ccc2c3c1ccc1c3c(cc2)ccc1

Computed Properties

• Complexity: 300
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• XLogP3: 5.7

Upstream Synthesis Route

1-Bromopyrene is a versatile chemical compound commonly used in organic synthesis for its unique reactivity and functional group compatibility. As a substituted pyrene derivative, 1-Bromopyrene serves as a valuable building block in the preparation of various complex organic molecules and materials.Its strategic bromine substituent allows for selective functionalization at the pyrene core, facilitating diverse chemical transformations and enabling the synthesis of novel compounds with specific properties and functionalities. In particular, 1-Bromopyrene is employed as a key intermediate in the synthesis of polycyclic aromatic hydrocarbons, which are essential in the development of organic semiconductors, materials science, and pharmaceutical research.Furthermore, the presence of the bromine atom enhances the electrophilicity of the pyrene ring, enabling efficient coupling reactions and facilitating the formation of carbon-carbon bonds in intricate molecular architectures. By leveraging the unique reactivity of 1-Bromopyrene, chemists can access a wide range of structurally complex molecules with tailored properties for various applications in the fields of organic chemistry and material science.

Literature

• Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chlorides.

  Journal of the American Chemical Society 20120411

• Luminescent ethynyl-pyrene liquid crystals and gels for optoelectronic devices.

  Journal of the American Chemical Society 20091223

• Synthesis, duplex-forming ability and fluorescent property of OligoDNA bearing silylated fluorophore.

  Nucleic acids symposium series (2004) 20070101

• Synthesis and photophysical characteristics of 2,7-fluorenevinylene-based trimers and their electroluminescence.

  The journal of physical chemistry. B 20061019