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(S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride

Base Information
  • Chemical Name:(S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride
  • CAS No.:1264239-56-6
  • Molecular Formula:C16H21NO4*ClH
  • Molecular Weight:327.808
  • Hs Code.:
(S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride

Synonyms:(S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride

Suppliers and Price of (S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride
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
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Total 3 raw suppliers
Chemical Property of (S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride

There total 7 articles about (S)-5-allyl 1-benzyl 2-(methylamino)pentanedioate hydrochloride 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: sodium hydrogencarbonate / N,N-dimethyl-formamide / 1 h / 20 °C
1.2: 16 h
2.1: hydrogenchloride / 1,4-dioxane / 1 h
3.1: pyridine / dichloromethane / 15 h / 0 °C
4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 4 h / 0 - 20 °C
5.1: thiophenol; caesium carbonate / acetonitrile / 16 h / 20 °C
5.2: 0.08 h
With pyridine; hydrogenchloride; sodium hydrogencarbonate; caesium carbonate; thiophenol; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 1 h / 20 °C
1.2: 16 h
2.1: hydrogenchloride / 1,4-dioxane / 1 h
3.1: pyridine / dichloromethane / 15 h / 0 °C
4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 4 h / 0 - 20 °C
5.1: thiophenol; caesium carbonate / acetonitrile / 16 h / 20 °C
5.2: 0.08 h
With pyridine; hydrogenchloride; sodium hydrogencarbonate; caesium carbonate; thiophenol; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
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