1,3,6-Tribromo-9H-carbazole

Base Information

• Chemical Name: 1,3,6-Tribromo-9H-carbazole
• CAS No.: 55119-10-3
• Molecular Formula: C12H6Br3N
• Molecular Weight: 403.898
• NSC Number: 121207
• DSSTox Substance ID: DTXSID20298164
• Nikkaji Number: J1.352.745H
• Wikidata: Q82039804
• Mol file: 55119-10-3.mol

Synonyms:1,3,6-Tribromo-9H-carbazole;55119-10-3;1,3,6-Tribromcarbazol;NSC121207;Cyto2F4;Maybridge1_002067;HMS547F21;DTXSID20298164;STK945984;AKOS000678164;CCG-234072;NSC 121207;NSC-121207;CS-0331791;A913802;SR-01000397425;SR-01000397425-1;BRD-K91956494-001-01-9

Chemical Property of 1,3,6-Tribromo-9H-carbazole

Chemical Property:

• Vapor Pressure: 1.14E-09mmHg at 25°C
• Melting Point: 184 °C
• Boiling Point: 500.8°C at 760 mmHg
• PKA: 14.60±0.30(Predicted)
• Flash Point: 256.7°C
• PSA: 15.79000
• Density: 2.188g/cm³
• LogP: 5.60860
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 402.80299
• Heavy Atom Count: 16
• Complexity: 273

Purity/Quality:

97% ^*data from raw suppliers

1,3,6-Tribromo-9H-carbazole 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=C(C=C1Br)C3=C(N2)C(=CC(=C3)Br)Br
• Uses: 1,3,6-Tribromo-9H-carbazole is a standard for environment and research. Carbazole-based hole transporting material and it’s application to the cost effective and environment friendly perovskite solar cells. An aryl hydrocarbon receptor agonist. Substance for the characterization and biological potency of mono- to tetra-halogenated carbazoles.

Technology Process of 1,3,6-Tribromo-9H-carbazole

There total 1 articles about 1,3,6-Tribromo-9H-carbazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

9H-carbazole (86-74-8,105184-46-1,97960-57-1) → 3,6-dibromo-9H-carbazole (6825-20-3) + 1,3,6-tribromo-9H-carbazole (55119-10-3) + 1,3,6,8-tetrabromo-9-methyl-9H-carbazole (55119-09-0)

Guidance literature:

With N-Bromosuccinimide; silica gel; In dichloromethane; at 18 ℃; for 72h; Yield given. Yields of byproduct given;

DOI:10.1016/S0040-4020(01)90362-X

Reference yield:

1,3,6-tribromo-9H-carbazole (55119-10-3) → 1,3,6,8-tetrabromo-9-methyl-9H-carbazole (55119-09-0)

Guidance literature:

With bromine; acetic acid;

Reference yield:

1,3,6-tribromo-9H-carbazole (55119-10-3) + bromine (7726-95-6) + acetic acid (64-19-7,77671-22-8) → 1,3,6,8-tetrabromo-9-methyl-9H-carbazole (55119-09-0)

Guidance literature:

upstream raw materials:

9H-carbazole

Downstream raw materials:

1,3,6,8-tetrabromo-9-methyl-9H-carbazole

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