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(R)-1-(3-methoxyphenyl)propan-2-amine

Base Information
  • Chemical Name:(R)-1-(3-methoxyphenyl)propan-2-amine
  • CAS No.:66033-00-9
  • Molecular Formula:C10H15NO
  • Molecular Weight:165.235
  • Hs Code.:
(R)-1-(3-methoxyphenyl)propan-2-amine

Synonyms:(R)-1-(3-methoxyphenyl)propan-2-amine

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Chemical Property of (R)-1-(3-methoxyphenyl)propan-2-amine
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Technology Process of (R)-1-(3-methoxyphenyl)propan-2-amine

There total 4 articles about (R)-1-(3-methoxyphenyl)propan-2-amine 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 glucose dehydrogenase; D-Alanine; D-glucose; NAD; lactate dehydrogenase; In aq. phosphate buffer; dimethyl sulfoxide; at 30 ℃; pH=7; Reagent/catalyst; enantioselective reaction; Enzymatic reaction;
DOI:10.1016/j.tetasy.2013.05.003
Guidance literature:
With formate dehydrogenase from Candida boidinii; alcohol dehydrogenase from Thermoanaerobacter ethanolicus W110A variant; amine dehydrogenase variant originated from the phenylalanine dehydrogenasefrom Rhodoccoccus species; NADPH oxidase from Bacillus subtilis; wild‐type alcohol dehydrogenase from Lactobacillus brevis; nicotinamide adenine dinucleotide phosphate; nicotinamide adenine dinucleotide; catalase; In aq. buffer; at 30 ℃; for 24h; pH=8.5; stereospecific reaction; Enzymatic reaction;
DOI:10.1039/c7ob01927k
Guidance literature:
With formate dehydrogenase from Candida boidinii; alcohol dehydrogenase from Thermoanaerobacter ethanolicus W110A variant; amine dehydrogenase variant originated from the phenylalanine dehydrogenasefrom Rhodoccoccus species; NADPH oxidase from Bacillus subtilis; nicotinamide adenine dinucleotide phosphate; nicotinamide adenine dinucleotide; catalase; In aq. buffer; at 30 ℃; for 24h; pH=8.5; stereospecific reaction; Enzymatic reaction;
DOI:10.1039/c7ob01927k
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