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{2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol

Base Information Edit
  • Chemical Name:{2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol
  • CAS No.:4745-77-1
  • Molecular Formula:C16H15N
  • Molecular Weight:221.302
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60963844
  • Mol file:4745-77-1.mol
{2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol

Synonyms:4745-77-1;Maybridge3_000866;DTXSID60963844;HMS1433H08;{2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol;IDI1_012253

Suppliers and Price of {2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol
Supply Marketing:Edit
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
Total 1 raw suppliers
Chemical Property of {2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol Edit
Chemical Property:
  • Vapor Pressure:1.65E-05mmHg at 25°C 
  • Boiling Point:350.4°Cat760mmHg 
  • Flash Point:165.7°C 
  • Density:1.4g/cm3 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:3
  • Exact Mass:258.06384051
  • Heavy Atom Count:17
  • Complexity:316
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1(CSC(=N1)NC2=C(C=C(C=C2)F)F)CO
Technology Process of {2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol

There total 8 articles about {2-[(2,4-Difluorophenyl)imino]-4-methyl-1,3-thiazolidin-4-yl}methanol 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: 58.0%

Guidance literature:
C16H14BrN; With bis(η3-allyl-μ-chloropalladium(II)); potassium carbonate; triphenylphosphine; In toluene; at 120 ℃; Inert atmosphere;
With sodium tetrahydroborate; In tetrahydrofuran; at 20 ℃; for 4h; Inert atmosphere;
DOI:10.1021/ol301663h
Guidance literature:
C16H14BrN; With bis(η3-allyl-μ-chloropalladium(II)); potassium carbonate; triphenylphosphine; In 1,4-dioxane; Reflux;
With sodium tetrahydroborate; In 1,4-dioxane; at 20 ℃;
DOI:10.1021/ol301663h
Guidance literature:
Multi-step reaction with 4 steps
1.1: potassium tert-butylate / tetrahydrofuran / 20 °C / Inert atmosphere
2.1: palladium on activated charcoal; hydrogen / ethyl acetate / 20 °C
3.1: water; sodium hydroxide / methanol / Reflux; Inert atmosphere
4.1: bis(η3-allyl-μ-chloropalladium(II)); potassium carbonate; triphenylphosphine / toluene / 120 °C / Inert atmosphere
4.2: 4 h / 20 °C / Inert atmosphere
With bis(η3-allyl-μ-chloropalladium(II)); palladium on activated charcoal; potassium tert-butylate; water; hydrogen; potassium carbonate; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; methanol; ethyl acetate; toluene; 1.1: Wittig olefination;
DOI:10.1021/ol301663h
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