Production Method 1

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  rt; 2 h, rt

Reference

Synthesis and characterization of a thiadiazole/benzimidazole-based copolymer for solar cell applications

Chen, Guan-yu; Lan, Shang-che; Lin, Po-yu; Chu, Chih-wei; Wei, Kung-hwa, Journal of Polymer Science, 2010, 48(20), 4456-4464

Production Method 2

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  0 °C; 2 h, 0 °C

Reference

Synthesis and structure-property relationship of carbazole-alt-benzothiadiazole copolymers

Oriou, Jules; Ng, Feifei; Hadziioannou, Georges; Brochon, Cyril; Cloutet, Eric, Journal of Polymer Science, 2015, 53(17), 2059-2068

Production Method 3

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  rt; 0 °C

Reference

polycarbazole-polyoxadiazole-based light emitting polymers with good luminescent efficiency and stability for light emitting devices

, Korea, , ,

Production Method 4

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  0 °C; 20 h, rt

Reference

Monomer and electroluminescent polymer, its preparation method and application

, China, , ,

Production Method 5

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Triethylamine, hydrochloride Solvents: Dichloromethane ;  90 min, rt

Reference

Quinoxaline-based organic semiconductor compound for organic solar cell and organic thin film transistor, manufacturing method thereof, and organic electronic device thereof

, Korea, , ,

Production Method 6

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Triethylamine, hydrochloride Solvents: Dichloromethane ;  0 °C; 90 min, 0 °C

Reference

Organic semiconductor material and photovoltaic device with it

, Korea, , ,

Production Method 7

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  0 °C; 0 °C → rt; overnight, rt

Reference

Bridging Small Molecules to Conjugated Polymers: Efficient Thermally Activated Delayed Fluorescence with a Methyl-Substituted Phenylene Linker

Rao, Jiancheng; Liu, Xinrui; Li, Xuefei; Yang, Liuqing; Zhao, Lei; et al, Angewandte Chemie, 2020, 59(3), 1320-1326

Production Method 8

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  0 - 5 °C
1.2 Solvents: Dichloromethane ;  0 - 5 °C; 90 min, 0 - 5 °C
1.3 Reagents: Water

Reference

Production of organic semiconductor material containing amine oxide group for OLED

, China, , ,

Production Method 9

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  0 - 5 °C
1.2 Solvents: Dichloromethane ;  90 min, 0 - 5 °C

Reference

Conjugated polyelectrolyte photoelectric material based on polycarbazole and its application

, China, , ,

Production Method 10

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  2 h, 0 °C
1.2 Solvents: Water ;  rt

Reference

A General and Air-tolerant Strategy to Conjugated Polymers within Seconds under Palladium(I) Dimer Catalysis

Magnin, Guillaume; Clifton, Jamie; Schoenebeck, Franziska, Angewandte Chemie, 2019, 58(30), 10179-10183

Production Method 11

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine ,  Trimethylammonium chloride Solvents: Dichloromethane ;  0 °C; 90 min, 0 °C

Reference

Carbazole nematic liquid crystals

Bao, Weixiao; Reddy Billa, Muralidhar; Kassireddy, Krishna; Haro, Marta; Kelly, Michael J.; et al, Liquid Crystals, 2010, 37(10), 1289-1303

Production Method 12

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Triethylamine Solvents: Dichloromethane ;  rt; 2 h, rt

Reference

Carbazole-based π-conjugated polyazomethines: Effects of catenation and comonomer insertion on optoelectronic features

Garbay, G.; Muccioli, L.; Pavlopoulou, E.; Hanifa, A.; Hadziioannou, G.; et al, Polymer, 2017, 119, 274-284

Production Method 13

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Pyridine ,  Triethylamine Solvents: Dichloromethane ;  1 h, 0 °C; 12 h, rt
1.2 Solvents: Water ;  30 min, rt

Reference

Conjugated polymers and their electron-donating organic materials, photovoltaic element materials, and photovoltaic elements

, Japan, , ,

Production Method 14

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Pyridine ,  Triethylamine Solvents: Dichloromethane ;  0 °C; 1 h, 0 °C; 12 h, rt

Reference

Carbon nanotube composites, organic semiconductor composites, and field-effect transistors

, World Intellectual Property Organization, , ,

Production Method 15

624-08-8

949898-99-1

Reaction Conditions

1.1 Reagents: Pyridine Catalysts: 4-(Dimethylamino)pyridine Solvents: Pyridine ;  0 °C; 10 min, 0 °C; 0 °C → rt; 8 h, rt

Reference

Synthesis and biological evaluation of galactofuranosyl alkyl thio-glycosides as inhibitors of Mycobacteria

Davis, Chris B.; Hartnell, Regan D.; Madge, Paul D.; Owen, David J.; Thomson, Robin J.; et al, Carbohydrate Research, 2007, 342(12-13), 1773-1780

heptadecan-9-yl 4-methylbenzenesulfonate Raw materials

• Heptadecan-9-ol

heptadecan-9-yl 4-methylbenzenesulfonate Preparation Products

• heptadecan-9-yl 4-methylbenzenesulfonate (949898-99-1)

• 1. Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
  Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
• 2. Embedding cyclic nitrone in mesoporous silica particles for EPR spin trapping of superoxide and other radicals?
  Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
• 3. Emerging investigators
  Polym. Chem., 2015,6, 5501-5502
• 4. Evolved polymerases facilitate selection of fully 2′-OMe-modified aptamers?
  Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
• 5. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293

• 5011-57-4(2-Heptanol, 4-methylbenzenesulfonate)
• 6522-44-7(1,5-Cyclooctanediol, bis(4-methylbenzenesulfonate), cis-)
• 6597-09-7(Cyclooctanol, 4-methylbenzenesulfonate)
• 62821-12-9(1,4-Cyclooctanediol, bis(4-methylbenzenesulfonate), cis- (9CI))
• 96243-68-4(2,4-Pentanediol, 2,4-bis(4-methylbenzenesulfonate), (2S,4S)-)
• 62821-09-4(1,4-Cycloheptanediol, bis(4-methylbenzenesulfonate), cis- (9CI))
• 1028-12-2(4-methylbenzenesulfonic Acid;octan-2-ol)
• 103576-23-4(2-Pentanol, 4-methylbenzenesulfonate, (S)-)
• 3813-69-2(pentan-2-yl 4-methylbenzenesulfonate)
• 6278-68-8(2,5-Hexanediol,2,5-bis(4-methylbenzenesulfonate))