6825-20-3 | 3,6-Dibromocarbazole

Packsize	Purity	Availability	Price	Discounted Price
25g	97%	in stock	$13.00	$9.00
100g	97%	in stock	$31.00	$22.00

Description

• Catalog Number: AB64041
• Chemical Name: 3,6-Dibromocarbazole
• CAS Number: 6825-20-3
• Molecular Formula: C12H7Br2N
• Molecular Weight: 324.9987
• MDL Number: MFCD00004961
• SMILES: Brc1ccc2c(c1)c1cc(Br)ccc1[nH]2
• NSC Number: 121206

Computed Properties

• Complexity: 222
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Donor Count: 1
• XLogP3: 4.8

Upstream Synthesis Route

3,6-Dibromo-9H-carbazole is a versatile compound that finds common application in chemical synthesis processes. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural properties. One of the primary uses of 3,6-Dibromo-9H-carbazole is as a key intermediate in the synthesis of organic materials such as liquid crystals, pharmaceuticals, and organic semiconductors. Its brominated structure plays a crucial role in facilitating further functionalization reactions, allowing chemists to tailor the compound for specific applications. Additionally, 3,6-Dibromo-9H-carbazole can serve as a precursory material for the development of novel polymers with desirable properties. Its ability to undergo diverse chemical transformations makes it a valuable tool in the toolkit of synthetic chemists seeking to innovate and create new materials with advanced functionalities.

Literature

• 5-(3,6-Dibromo-9H-carbazol-9-yl)penta-nenitrile.

  Acta crystallographica. Section E, Structure reports online 20110301

• 3,6-Dibromo-9-(4-chloro-benz-yl)-9H-carbazole.

  Acta crystallographica. Section E, Structure reports online 20090201

• 3,6-Dibromo-9-(4-bromo-benz-yl)-9H-carbazole.

  Acta crystallographica. Section E, Structure reports online 20090201

• 3,6-Dibromo-9-(4-tert-butyl-benz-yl)-9H-carbazole.

  Acta crystallographica. Section E, Structure reports online 20080801

• Novel multicomponent reactions involving isoquinoline or phenanthridine and activated acetylenic ester in the presence of heterocyclic NH or 1,3-dicarbonyl compounds.

  Molecular diversity 20080501

• Synthesis and activity of carbazole derivatives against Mycobacterium tuberculosis.

  ChemMedChem 20060801

• Determination of N-NO bond dissociation energies of N-methyl-N-nitrosobenzenesulfonamides in acetonitrile and application in the mechanism analyses on NO transfer.

  Journal of the American Chemical Society 20050302

• Density functional theory studies on the structures and vibrational spectra of 3,6-dichlorocarbazole and 3,6-dibromocarbazole.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20020801