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D-102 Dye

Base Information
  • Chemical Name:D-102 Dye
  • CAS No.:652145-28-3
  • Molecular Formula:C37H30N2O3S2
  • Molecular Weight:614.789
  • Hs Code.:
  • Mol file:652145-28-3.mol
D-102 Dye

Synonyms:D-102 Dye;

Suppliers and Price of D-102 Dye
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • D102 Dye
  • 25mg
  • $ 1595.00
  • TCI Chemical
  • D 102 >96.0%(HPLC)
  • 50mg
  • $ 137.00
  • Sigma-Aldrich
  • D102 Dye 95% (HPLC)
  • 200mg
  • $ 311.00
  • Arctom
  • D 102 ≥98%
  • 1g
  • $ 814.00
  • Arctom
  • D 102 ≥98%
  • 250mg
  • $ 327.00
  • Arctom
  • D 102 ≥98%
  • 100mg
  • $ 218.00
  • AK Scientific
  • 2-[5-[[4-[4-(2,2-Diphenylvinyl)phenyl]-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indol-7-yl]methylene]-4-oxo-2-thioxothiazolidin-3-yl]aceticacid
  • 50mg
  • $ 221.00
Total 9 raw suppliers
Chemical Property of D-102 Dye
Chemical Property:
  • Melting Point:238-243°C 
  • PSA:118.24000 
  • Density:1.42±0.1 g/cm3 (20 oC 760 Torr), Calc.* 
  • LogP:8.35200 
Purity/Quality:

97% *data from raw suppliers

D102 Dye *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn 
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Organic dye for highly efficient solid-state dye-sensitized solar cells. D102 Dye can be used as a sensitizing material that can be coated on the semiconducting electrode for the fabrication of metal-free dye sensitized solar cells.
Technology Process of D-102 Dye

There total 7 articles about D-102 Dye 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:
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium tetrahydroborate; acetic acid / 20 °C
2.1: tri-tert-butyl phosphine; potassium tert-butylate; palladium diacetate / 5,5-dimethyl-1,3-cyclohexadiene / 120 °C
3.1: trichlorophosphate / 10 °C
3.2: 20 °C
4.1: ammonium acetate; acetic acid / 120 °C
With sodium tetrahydroborate; tri-tert-butyl phosphine; potassium tert-butylate; ammonium acetate; palladium diacetate; acetic acid; trichlorophosphate; In 5,5-dimethyl-1,3-cyclohexadiene;
DOI:10.1016/j.dyepig.2011.02.009
Guidance literature:
Multi-step reaction with 3 steps
1.1: tri-tert-butyl phosphine; potassium tert-butylate; palladium diacetate / 5,5-dimethyl-1,3-cyclohexadiene / 120 °C
2.1: trichlorophosphate / 10 °C
2.2: 20 °C
3.1: ammonium acetate; acetic acid / 120 °C
With tri-tert-butyl phosphine; potassium tert-butylate; ammonium acetate; palladium diacetate; acetic acid; trichlorophosphate; In 5,5-dimethyl-1,3-cyclohexadiene;
DOI:10.1016/j.dyepig.2011.02.009
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium acetate; acetic acid / dichloromethane; water / 2 h / Reflux
2.1: sodium tetrahydroborate; acetic acid / 20 °C
3.1: tri-tert-butyl phosphine; potassium tert-butylate; palladium diacetate / 5,5-dimethyl-1,3-cyclohexadiene / 120 °C
4.1: trichlorophosphate / 10 °C
4.2: 20 °C
5.1: ammonium acetate; acetic acid / 120 °C
With sodium tetrahydroborate; tri-tert-butyl phosphine; potassium tert-butylate; ammonium acetate; sodium acetate; palladium diacetate; acetic acid; trichlorophosphate; In 5,5-dimethyl-1,3-cyclohexadiene; dichloromethane; water;
DOI:10.1016/j.dyepig.2011.02.009
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