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(R,S)-3-hydroxy-4-<<3-(propylamino)-3-oxopropyl>thio>-2,2-dimethyl-4-oxobutan-1-ol, phosphate ester

Base Information
  • Chemical Name:(R,S)-3-hydroxy-4-<<3-(propylamino)-3-oxopropyl>thio>-2,2-dimethyl-4-oxobutan-1-ol, phosphate ester
  • CAS No.:223710-71-2
  • Molecular Formula:C12H24NO7PS
  • Molecular Weight:357.365
  • Hs Code.:
(R,S)-3-hydroxy-4-<<3-(propylamino)-3-oxopropyl>thio>-2,2-dimethyl-4-oxobutan-1-ol, phosphate ester

Synonyms:(R,S)-3-hydroxy-4-<<3-(propylamino)-3-oxopropyl>thio>-2,2-dimethyl-4-oxobutan-1-ol, phosphate ester

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Chemical Property of (R,S)-3-hydroxy-4-<<3-(propylamino)-3-oxopropyl>thio>-2,2-dimethyl-4-oxobutan-1-ol, phosphate ester
Chemical Property:
Purity/Quality:
Safty Information:
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Technology Process of (R,S)-3-hydroxy-4-<<3-(propylamino)-3-oxopropyl>thio>-2,2-dimethyl-4-oxobutan-1-ol, phosphate ester

There total 1 articles about (R,S)-3-hydroxy-4-<<3-(propylamino)-3-oxopropyl>thio>-2,2-dimethyl-4-oxobutan-1-ol, phosphate 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 4 steps
1: 97 percent / diethyl ether / Ambient temperature
2: 94 percent / sodium methoxide / methanol / 1 h / Ambient temperature
3: 51 percent / CsF / tetrahydrofuran / 48 h
4: 87 percent / trimethylsilyl chloride, tetrabutylammonium bromide / acetonitrile / 15 h / 40 °C
With chloro-trimethyl-silane; tetrabutylammomium bromide; sodium methylate; cesium fluoride; In tetrahydrofuran; methanol; diethyl ether; acetonitrile;
DOI:10.1021/jo981758s
Guidance literature:
Multi-step reaction with 3 steps
1: 56 percent / phosphopantetheine adenylyltransferase, dephosphocoenzyme A kinase, MgCl2, pyrophosphatase, pyruvate kinase, phospho(enol) pyruvate / H2O; various solvent(s) / 168 h / Ambient temperature
2: Crotalus atrox venom nucleotide pyrophosphatase EC 3.6.1.9 / H2O / 4 h
3: potato acid phosphatase EC 3.1.3.2 / H2O / 21 h
With pyrophosphatase; pyruvate kinase; Crotalus atrox venom nucleotide pyrophosphatase EC 3.6.1.9; dephosphocoenzyme A kinase; phospho(enol) pyruvate; phosphopantetheine adenylyltransferase; potato acid phosphatase EC 3.1.3.2; magnesium chloride; In water;
DOI:10.1021/jo981758s
Guidance literature:
Multi-step reaction with 4 steps
1: 56 percent / phosphopantetheine adenylyltransferase, dephosphocoenzyme A kinase, MgCl2, pyrophosphatase, pyruvate kinase, phospho(enol) pyruvate / H2O; various solvent(s) / 168 h / Ambient temperature
2: Crotalus atrox venom nucleotide pyrophosphatase EC 3.6.1.9 / H2O / 4 h
3: potato acid phosphatase EC 3.1.3.2 / H2O / 21 h
4: pyridine
With pyridine; pyrophosphatase; pyruvate kinase; Crotalus atrox venom nucleotide pyrophosphatase EC 3.6.1.9; dephosphocoenzyme A kinase; phospho(enol) pyruvate; phosphopantetheine adenylyltransferase; potato acid phosphatase EC 3.1.3.2; magnesium chloride; In water;
DOI:10.1021/jo981758s
upstream raw materials:

N-propylacrylamide

Downstream raw materials:

(R)-Pantolacton

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