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2,5-Dibenzyloxyphenylacetic acid

Base Information
  • Chemical Name:2,5-Dibenzyloxyphenylacetic acid
  • CAS No.:79755-47-8
  • Molecular Formula:C22H20 O4
  • Molecular Weight:348.39
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60564214
  • Wikidata:Q82448832
  • Mol file:79755-47-8.mol
2,5-Dibenzyloxyphenylacetic acid

Synonyms:2,5-DIBENZYLOXYPHENYLACETIC ACID;79755-47-8;2-[2,5-bis(phenylmethoxy)phenyl]acetic acid;2,5-Dibenzyloxyphenylaceticacid;SCHEMBL7823412;DTXSID60564214;2-(2,5-Bis(benzyloxy)phenyl)acetic acid;[2,5-BIS(BENZYLOXY)PHENYL]ACETIC ACID

Suppliers and Price of 2,5-Dibenzyloxyphenylacetic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Biosynth Carbosynth
  • 2,5-Dibenzyloxyphenylacetic acid
  • 25 g
  • $ 250.00
  • Biosynth Carbosynth
  • 2,5-Dibenzyloxyphenylacetic acid
  • 10 g
  • $ 125.00
  • Biosynth Carbosynth
  • 2,5-Dibenzyloxyphenylacetic acid
  • 5 g
  • $ 75.00
Total 4 raw suppliers
Chemical Property of 2,5-Dibenzyloxyphenylacetic acid
Chemical Property:
  • PSA:55.76000 
  • LogP:4.47170 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:8
  • Exact Mass:348.13615911
  • Heavy Atom Count:26
  • Complexity:412
Purity/Quality:

99% *data from raw suppliers

2,5-Dibenzyloxyphenylacetic acid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COC2=CC(=C(C=C2)OCC3=CC=CC=C3)CC(=O)O
Technology Process of 2,5-Dibenzyloxyphenylacetic acid

There total 8 articles about 2,5-Dibenzyloxyphenylacetic 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 sodium hydroxide; In ethanol; Heating;
DOI:10.1039/P19810002570
Guidance literature:
Multi-step reaction with 6 steps
1: potassium carbonate / butan-2-one / 16 h / Heating
2: aq. NaOH / ethanol / Heating
3: 80 percent / LiAlH4 / tetrahydrofuran / Heating
4: 90 percent / thionyl chloride, pyridine / diethyl ether
5: 65 percent / Heating
6: 75 percent / aq. NaOH / ethanol / Heating
With pyridine; sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; In tetrahydrofuran; diethyl ether; ethanol; butanone;
DOI:10.1039/P19810002570
Guidance literature:
Multi-step reaction with 4 steps
1: 80 percent / LiAlH4 / tetrahydrofuran / Heating
2: 90 percent / thionyl chloride, pyridine / diethyl ether
3: 65 percent / Heating
4: 75 percent / aq. NaOH / ethanol / Heating
With pyridine; sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; diethyl ether; ethanol;
DOI:10.1039/P19810002570
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