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1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester

Base Information Edit
  • Chemical Name:1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester
  • CAS No.:69937-82-2
  • Molecular Formula:C33H29N3O2
  • Molecular Weight:499.60200
  • Hs Code.:
  • Mol file:69937-82-2.mol
1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester

Synonyms:

Suppliers and Price of 1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester
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
  • TRC
  • 1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidineMethylEster
  • 50mg
  • $ 165.00
  • Medical Isotopes, Inc.
  • 1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidineMethylEster
  • 50 mg
  • $ 650.00
Total 0 raw suppliers
Chemical Property of 1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester Edit
Chemical Property:
  • PSA:56.48000 
  • LogP:5.92650 
  • Storage Temp.:-20°C Freezer, Under inert atmosphere 
Purity/Quality:

1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidineMethylEster *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester can be used in the preparation of optically pure L-(+)-Ergothioneine. L-Histidine Methyl Ester (H456020) derivative. Used in the preparation of optically pure L-(+)-Ergothioneine.
Technology Process of 1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester

There total 8 articles about 1-(Triphenylmethyl)-N-(phenylmethylene)-L-histidine Methyl Ester 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 3 steps
1: 99 percent / Et3N / benzene / 1 h / 80 °C
2: 0.78 g / H2 / 10percent Pd/C / methanol / 2.5 h / 25 °C / 760 Torr
3: methanol / 1.5 h / 25 °C
With hydrogen; triethylamine; palladium on activated charcoal; In methanol; benzene;
DOI:10.1016/0968-0896(95)00183-2
Guidance literature:
Multi-step reaction with 4 steps
1: 80 percent / 1N aq. NaOH / methanol / 0.01 h / -20 °C
2: 99 percent / Et3N / benzene / 1 h / 80 °C
3: 0.78 g / H2 / 10percent Pd/C / methanol / 2.5 h / 25 °C / 760 Torr
4: methanol / 1.5 h / 25 °C
With sodium hydroxide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; benzene;
DOI:10.1016/0968-0896(95)00183-2
Guidance literature:
Multi-step reaction with 6 steps
1: 99 percent / SOCl2 / 36 h / 40 °C
2: 49 percent / aq. NaHCO3 / acetone / 12 h / 25 °C
3: 80 percent / 1N aq. NaOH / methanol / 0.01 h / -20 °C
4: 99 percent / Et3N / benzene / 1 h / 80 °C
5: 0.78 g / H2 / 10percent Pd/C / methanol / 2.5 h / 25 °C / 760 Torr
6: methanol / 1.5 h / 25 °C
With sodium hydroxide; thionyl chloride; hydrogen; sodium hydrogencarbonate; triethylamine; palladium on activated charcoal; In methanol; acetone; benzene;
DOI:10.1016/0968-0896(95)00183-2
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