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2-(2-Hydroxyphenyl)propionic acid

Base Information
  • Chemical Name:2-(2-Hydroxyphenyl)propionic acid
  • CAS No.:533931-68-9
  • Molecular Formula:C9H10O3
  • Molecular Weight:166.177
  • Hs Code.:
  • UNII:SS74MY8K8F
2-(2-Hydroxyphenyl)propionic acid

Synonyms:2-(2-HYDROXYPHENYL)PROPIONIC ACID;2-(2-Hydroxyphenyl)propanoic acid;533931-68-9;SS74MY8K8F;UNII-SS74MY8K8F;2-(2-Hydroxyphenyl)propanoic acid, (+/-)-;2-(2-Hydroxy-phenyl)-propionic acid;2-Hydroxy-alpha-methylbenzeneacetic acid;Benzeneacetic acid, 2-hydroxy-alpha-methyl-;2-hydroxyphenylpropanoic acid;SCHEMBL153695;KRHQRJXHSUXNQY-UHFFFAOYSA-N;2-(2-Hydroxyphenyl)-propionic acid;MFCD20641531;EN300-1847666;2-HYDROXY-.ALPHA.-METHYLBENZENEACETIC ACID;BENZENEACETIC ACID, 2-HYDROXY-.ALPHA.-METHYL-

Suppliers and Price of 2-(2-Hydroxyphenyl)propionic acid
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Chemical Property of 2-(2-Hydroxyphenyl)propionic acid
Chemical Property:
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:166.062994177
  • Heavy Atom Count:12
  • Complexity:167
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C1=CC=CC=C1O)C(=O)O
Technology Process of 2-(2-Hydroxyphenyl)propionic acid

There total 7 articles about 2-(2-Hydroxyphenyl)propionic acid 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 hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00113a027
Guidance literature:
Multi-step reaction with 3 steps
1: 95 percent / CaCl2, conc. HCl / dioxane / 1 h / Ambient temperature
2: 2.) 2 N aq. KOH / 1.) DMSO, reflux, 1 h , 2.) ethanol, reflux, overnight
3: 100 percent / H2 / Pd/C / ethanol
With hydrogenchloride; potassium hydroxide; hydrogen; calcium chloride; palladium on activated charcoal; In 1,4-dioxane; ethanol;
DOI:10.1021/jm00113a027
Guidance literature:
Multi-step reaction with 4 steps
1: 98 percent / NaBH4 / ethanol / 1 h / Heating
2: 95 percent / CaCl2, conc. HCl / dioxane / 1 h / Ambient temperature
3: 2.) 2 N aq. KOH / 1.) DMSO, reflux, 1 h , 2.) ethanol, reflux, overnight
4: 100 percent / H2 / Pd/C / ethanol
With hydrogenchloride; potassium hydroxide; sodium tetrahydroborate; hydrogen; calcium chloride; palladium on activated charcoal; In 1,4-dioxane; ethanol;
DOI:10.1021/jm00113a027
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