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EGF816 (mesylate)

Base Information
  • Chemical Name:EGF816 (mesylate)
  • CAS No.:1508250-72-3
  • Molecular Formula:(x)CH4O3S*C26H31ClN6O2
  • Molecular Weight:591.12
  • Hs Code.:
  • Mol file:1508250-72-3.mol
EGF816 (mesylate)

Synonyms:

Suppliers and Price of EGF816 (mesylate)
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
  • DC Chemicals
  • EGF816mesylate >98%
  • 1 g
  • $ 2400.00
  • DC Chemicals
  • EGF816mesylate >98%
  • 250 mg
  • $ 1200.00
  • DC Chemicals
  • EGF816mesylate >98%
  • 100 mg
  • $ 600.00
  • Crysdot
  • EGF816mesylate 98+%
  • 10mg
  • $ 347.00
  • Crysdot
  • EGF816mesylate 98+%
  • 5mg
  • $ 243.00
  • Crysdot
  • EGF816mesylate 98+%
  • 50mg
  • $ 1042.00
  • Crysdot
  • EGF816mesylate 98+%
  • 100mg
  • $ 1459.00
  • Biorbyt Ltd
  • EGF816 mesylate
  • 250 mg
  • $ 1802.00
  • Biorbyt Ltd
  • EGF816 mesylate
  • 100 mg
  • $ 912.90
Total 6 raw suppliers
Chemical Property of EGF816 (mesylate)
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

EGF816mesylate >98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of EGF816 (mesylate)

There total 12 articles about EGF816 (mesylate) 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 5 steps
1.1: HATU; triethylamine / dichloromethane / 1 h / 20 °C
1.2: 2.17 h
2.1: hydrogenchloride / methanol; 1,4-dioxane / 7 h / 20 °C
3.1: sodium hydroxide / ethyl acetate
4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 1 h / 20 °C
4.2: 120 h
5.1: acetone / 55 °C
With hydrogenchloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; HATU; sodium hydroxide; In 1,4-dioxane; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetone;
Guidance literature:
Multi-step reaction with 4 steps
1.1: triethylamine; HATU / dichloromethane / 1 h / 20 °C
1.2: 2 h
2.1: hydrogenchloride / methanol; 1,4-dioxane / 7 h / 20 °C
3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C
3.2: 120 h
4.1: acetone
With hydrogenchloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; HATU; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
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