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TC-E 5002

Base Information
  • Chemical Name:TC-E 5002
  • CAS No.:1453071-47-0
  • Molecular Formula:C15H27NO4
  • Molecular Weight:285.384
  • Hs Code.:
TC-E 5002

Synonyms:

Suppliers and Price of TC-E 5002
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
  • Usbiological
  • TC-E 5002
  • 10mg
  • $ 480.00
  • TRC
  • N-(9-Cyclopropyl-1-oxononyl)-N-hydroxy-β-alanine
  • 10mg
  • $ 185.00
  • Tocris
  • TC-E5002 ≥98%(HPLC)
  • 50
  • $ 952.00
  • Tocris
  • TC-E5002 ≥98%(HPLC)
  • 10
  • $ 227.00
  • TCI Chemical
  • N-(9-Cyclopropyl-1-oxononyl)-N-hydroxy-β-alanine >80.0%(HPLC)
  • 5mg
  • $ 210.00
  • Cayman Chemical
  • TC-E 5002 ≥98%
  • 50mg
  • $ 786.00
  • Cayman Chemical
  • TC-E 5002 ≥98%
  • 10mg
  • $ 185.00
  • Cayman Chemical
  • TC-E 5002 ≥98%
  • 5mg
  • $ 110.00
  • Cayman Chemical
  • TC-E 5002 ≥98%
  • 1mg
  • $ 26.00
  • ApexBio Technology
  • TC-E5002
  • 10mg
  • $ 329.00
Total 8 raw suppliers
Chemical Property of TC-E 5002
Chemical Property:
  • Melting Point:87°C(lit.) 
  • Boiling Point:457.3±47.0 °C(Predicted) 
  • Density:1.130±0.06 g/cm3(Predicted) 
Purity/Quality:

97% *data from raw suppliers

TC-E 5002 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses N-(9-Cyclopropyl-1-oxononyl)-N-hydroxy-β-alanine is a selective histone demethylase KDM2/7 inhibitor used in tumor inhibition and suppression of cancer cell growth.
Technology Process of TC-E 5002

There total 5 articles about TC-E 5002 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:
With hydrogenchloride; water; In 1,4-dioxane; dichloromethane; at 20 ℃; for 16h;
DOI:10.1021/jm400624b

Reference yield: 13.0%

Guidance literature:
With hydrogenchloride; In 1,4-dioxane; dichloromethane; at 20 ℃; for 13h; Cooling with ice;
Guidance literature:
Multi-step reaction with 4 steps
1.1: dilithium tetrachlorocuprate / tetrahydrofuran / 2 h / -10 °C
1.2: Acidic conditions
2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 15 h / 80 °C
3.1: 5%-palladium/activated carbon; hydrogen; ethyl acetate / 1 h / 20 °C
4.1: hydrogenchloride; water / 1,4-dioxane; dichloromethane / 16 h / 20 °C
With hydrogenchloride; dilithium tetrachlorocuprate; 5%-palladium/activated carbon; water; hydrogen; benzotriazol-1-ol; ethyl acetate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm400624b
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