2-Amino-1-(3-phenoxyphenyl)ethan-1-ol

Base Information

• Chemical Name: 2-Amino-1-(3-phenoxyphenyl)ethan-1-ol
• CAS No.: 133562-41-1
• Molecular Formula: C14H15NO2
• Molecular Weight: 265.74
• Hs Code.: 2922509090
• Nikkaji Number: J532.146H
• Mol file: 133562-41-1.mol

Synonyms:2-Amino-1-(3-phenoxyphenyl)ethan-1-ol;SCHEMBL2847175;BJTVAYZPBFANDH-UHFFFAOYSA-N;2-amino-1-(3-phenoxyphenyl)ethanol;2-amino-1-(3-phenoxyphenyl)-1-ethanol;CS-0352523;EN300-1863483

Chemical Property of 2-Amino-1-(3-phenoxyphenyl)ethan-1-ol

Chemical Property:

• PSA: 55.48000
• LogP: 3.97330
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 229.110278721
• Heavy Atom Count: 17
• Complexity: 216

Purity/Quality:

99% ^*data from raw suppliers

2-Amino-1-(3-phenoxyphenyl)ethanolhydrochloride 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)OC2=CC=CC(=C2)C(CN)O

Technology Process of 2-Amino-1-(3-phenoxyphenyl)ethan-1-ol

There total 1 articles about 2-Amino-1-(3-phenoxyphenyl)ethan-1-ol 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:

Reference yield:

2-hydroxy-2-(3-phenoxyphenyl)acetonitrile (39515-47-4) → 2-amino-1-(3-phenoxyphenyl)-1-ethanol (133562-41-1)

Guidance literature:

With sodium hydroxide; In tetrahydrofuran; water;

Reference yield: 67.0%

2-[1-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-propyl]-[1,3]dithiolane-2-carboxylic acid ethyl ester + 2-amino-1-(3-phenoxyphenyl)-1-ethanol (133562-41-1) → ((S)-1-{1-[2-Hydroxy-2-(3-phenoxy-phenyl)-ethylaminooxalyl]-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

Guidance literature:

In ethanol; Ambient temperature;

DOI:10.1021/jm950541c

Reference yield: 50.0%

2-[1-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-2-phenyl-ethyl]-[1,3]dithiolane-2-carboxylic acid ethyl ester + 2-amino-1-(3-phenoxyphenyl)-1-ethanol (133562-41-1) → ((S)-1-{1-Benzyl-2-[2-hydroxy-2-(3-phenoxy-phenyl)-ethylcarbamoyl]-2-oxo-ethylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

Guidance literature:

In ethanol; Ambient temperature;

DOI:10.1021/jm950541c

upstream raw materials:

2-hydroxy-2-(3-phenoxyphenyl)acetonitrile

Downstream raw materials:

5-((2S)-2-({(2S)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropanoyl}amino)-3-{[2-hydroxy-2-(3-phenoxyphenyl)ethyl]amino}-3-oxopropyl)-2-(carboxymethoxy)benzoic Acid

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