Production Method 1

1081-34-1

790712-85-5

118824-91-2

98057-08-0

Reaction Conditions

1.1R:C:FeCl3, S:CH2Cl2, 10 min, rt

Reference

Rapid and effective multihalogenations of 2,2',5',2''-terthiophene with 2-halo-4,5-dichloropyridazin-3(2H)-ones under ambient conditions

By Kim, Eun Jung et al, Bulletin of the Korean Chemical Society, 2010, 31(10), 2985-2988

Production Method 2

1081-34-1

790712-85-5

Reaction Conditions

1.1R:Br2, S:CHCl3, S:AcOH, 10°C; overnight, rt

Reference

Building Blocks for N-Type Molecular and Polymeric Electronics. Perfluoroalkyl- versus Alkyl-Functionalized Oligothiophenes (nTs; n = 2-6). Systematic Synthesis, Spectroscopy, Electrochemistry, and Solid-State Organization

By Facchetti, Antonio et al, Journal of the American Chemical Society, 2004, 126(41), 13480-13501

Production Method 3

1081-34-1

790712-85-5

Reaction Conditions

1.1R:AcOH, R:Bromosuccinimide, S:CHCl3, 10°C

Reference

A Terthiophene-Containing Alkynylplatinum Terpyridine Pacman Complex: Controllable Folding/Unfolding Modulated by Weak Intermolecular Interactions

By Cao, Yang et al, Inorganic Chemistry, 2013, 52(10), 5636-5638

Production Method 4

1081-34-1

790712-85-5

1261644-74-9

1261644-71-6

Reaction Conditions

1.1R:C:FeCl3, S:CH2Cl2, 10 min, rt

Reference

Rapid and effective multihalogenations of 2,2',5',2''-terthiophene with 2-halo-4,5-dichloropyridazin-3(2H)-ones under ambient conditions

By Kim, Eun Jung et al, Bulletin of the Korean Chemical Society, 2010, 31(10), 2985-2988

2,2':5',2''-Terthiophene, 3,3'',5,5''-tetrabromo- (9CI) Raw materials

• 2,2':5',2''-Terthiophene

2,2':5',2''-Terthiophene, 3,3'',5,5''-tetrabromo- (9CI) Preparation Products

• 2,4,5''-tribromo-2,2',5',2''-terthiophene (118824-91-2)
• 2,2':5',2''-Terthiophene, 3,3',3'',4',5,5''-hexabromo- (1261644-74-9)
• 2,2':5',2''-Terthiophene, 3,3'',5,5''-tetrabromo- (9CI) (790712-85-5)
• 2,2':5',2''-Terthiophene, 3,3',3'',5,5''-pentabromo- (1261644-71-6)
• 5,5''-Dibromo-2,2':5',2''-terthiophene (98057-08-0)

• 1. An inter-tangled network of redox-active and conducting polymers as a cathode for ultrafast rechargeable batteries
  Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon Song Phys. Chem. Chem. Phys., 2014,16, 5295-5300
• 2. An approach to biodegradable star polymeric architectures using disulfide coupling?
  Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
• 3. Acetyl group orientation modulates the electronic ground-state asymmetry of the special pair in purple bacterial reaction centers
  P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. Buda Phys. Chem. Chem. Phys., 2011,13, 10270-10279
• 4. An Appraisal of pH triggered Bacitracin drug release, through composite hydrogel systems
  RabailGul,MariamMir,MurtazaNAli
• 5. An air-stable organometallic polymer containing titanafluorene moieties obtained by the Sonogashira–Hagihara cross-coupling polycondensation?
  Alvin Tanudjaja,Shinsuke Inagi,Fusao Kitamura,Toshikazu Takata,Ikuyoshi Tomita Dalton Trans., 2021,50, 3037-3043

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)