3141-27-3 | 2,5-Dibromothiophene

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$8.00	$5.00
100g	98%	in stock	$9.00	$6.00
500g	98%	in stock	$25.00	$17.00
1kg	98%	in stock	$43.00	$30.00

Description

• Catalog Number: AB60392
• Chemical Name: 2,5-Dibromothiophene
• CAS Number: 3141-27-3
• Molecular Formula: C4H2Br2S
• Molecular Weight: 241.9317
• MDL Number: MFCD00005420
• SMILES: Brc1ccc(s1)Br
• NSC Number: 4488

Computed Properties

• Complexity: 58.7
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 3.7

Upstream Synthesis Route

2,5-Dibromothiophene is a versatile compound that is commonly used in chemical synthesis for a variety of applications. This compound serves as a building block in the preparation of various organic molecules, including pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex organic compounds. In particular, 2,5-Dibromothiophene is often employed in the development of new materials for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Additionally, it can be utilized in the preparation of specialty polymers and functionalized organic molecules. Its ability to undergo various chemical transformations, such as Suzuki cross-coupling reactions and palladium-catalyzed coupling reactions, make it an essential component in the toolbox of synthetic chemists. Overall, 2,5-Dibromothiophene plays a crucial role in the modern synthesis of organic compounds with diverse applications.

Literature

• Synthesis of functionalized thiophenes and oligothiophenes by selective and iterative cross-coupling reactions using indium organometallics.

  Organic & biomolecular chemistry 20120521

• Rhenium ethoxy- and hydroxycarbene complexes with thiophene substituents.

  Dalton transactions (Cambridge, England : 2003) 20111007

• 4,4'-[Thio-phene-2,5-diylbis(ethyne-2,1-di-yl)]dibenzonitrile.

  Acta crystallographica. Section E, Structure reports online 20080401

• Prediction of genotoxicity of chemical compounds by statistical learning methods.

  Chemical research in toxicology 20050601