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(3R,E)-3-amino-3-phenyl-1-phenylsulfonyl-1-propene trifluoroacetate salt

Base Information
  • Chemical Name:(3R,E)-3-amino-3-phenyl-1-phenylsulfonyl-1-propene trifluoroacetate salt
  • CAS No.:1253911-96-4
  • Molecular Formula:C2HF3O2*C15H15NO2S
  • Molecular Weight:387.38
  • Hs Code.:
(3R,E)-3-amino-3-phenyl-1-phenylsulfonyl-1-propene trifluoroacetate salt

Synonyms:(3R,E)-3-amino-3-phenyl-1-phenylsulfonyl-1-propene trifluoroacetate salt

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Chemical Property of (3R,E)-3-amino-3-phenyl-1-phenylsulfonyl-1-propene trifluoroacetate salt
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Technology Process of (3R,E)-3-amino-3-phenyl-1-phenylsulfonyl-1-propene trifluoroacetate salt

There total 7 articles about (3R,E)-3-amino-3-phenyl-1-phenylsulfonyl-1-propene trifluoroacetate salt 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 8 steps
1: titanium(IV) isopropylate; tert.-butylhydroperoxide; D-(-)-diisopropyl tartrate / 2,2,4-trimethylpentane; dichloromethane / Molecular sieve; Inert atmosphere
2: sodium azide; lithium perchlorate / acetonitrile
3: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 °C / 760.05 Torr
4: di-isopropyl azodicarboxylate; triphenylphosphine / chloroform / Reflux
5: triethylamine / methanol / Inert atmosphere; Reflux
6: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C
7: N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide p-toluenesulfonate; copper dichloride / acetonitrile
8: dichloromethane / 0.5 h / 20 °C
With titanium(IV) isopropylate; tert.-butylhydroperoxide; sodium azide; di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; lithium perchlorate; N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide p-toluenesulfonate; D-(-)-diisopropyl tartrate; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; copper dichloride; In methanol; 2,2,4-trimethylpentane; dichloromethane; chloroform; ethyl acetate; acetonitrile;
DOI:10.1002/cmdc.201000109
Guidance literature:
Multi-step reaction with 7 steps
1: sodium azide; lithium perchlorate / acetonitrile
2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 °C / 760.05 Torr
3: di-isopropyl azodicarboxylate; triphenylphosphine / chloroform / Reflux
4: triethylamine / methanol / Inert atmosphere; Reflux
5: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C
6: N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide p-toluenesulfonate; copper dichloride / acetonitrile
7: dichloromethane / 0.5 h / 20 °C
With sodium azide; di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; lithium perchlorate; N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide p-toluenesulfonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; copper dichloride; In methanol; dichloromethane; chloroform; ethyl acetate; acetonitrile;
DOI:10.1002/cmdc.201000109
Guidance literature:
Multi-step reaction with 6 steps
1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 °C / 760.05 Torr
2: di-isopropyl azodicarboxylate; triphenylphosphine / chloroform / Reflux
3: triethylamine / methanol / Inert atmosphere; Reflux
4: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C
5: N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide p-toluenesulfonate; copper dichloride / acetonitrile
6: dichloromethane / 0.5 h / 20 °C
With di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide p-toluenesulfonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; copper dichloride; In methanol; dichloromethane; chloroform; ethyl acetate; acetonitrile;
DOI:10.1002/cmdc.201000109
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