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3-Acetoxycinnamic acid

Base Information
  • Chemical Name:3-Acetoxycinnamic acid
  • CAS No.:20375-42-2
  • Molecular Formula:C11H10 O4
  • Molecular Weight:206.198
  • Hs Code.:2918990090
  • European Community (EC) Number:654-540-2
  • NSC Number:164923
  • Nikkaji Number:J1.581.302D
  • Wikidata:Q76305676
  • Mol file:20375-42-2.mol
3-Acetoxycinnamic acid

Synonyms:3-Acetoxycinnamic acid;20375-42-2;m-Acetyl coumaric acid;(E)-3-(3-acetyloxyphenyl)prop-2-enoic acid;2-Propenoic acid, 3-[3-(acetyloxy)phenyl]-;SCHEMBL1711133;LSZKRNUEKNCZIE-AATRIKPKSA-N;NSC164923;(E)-3-(3-acetoxyphenyl)acrylic acid;NSC 164923;NSC-164923;2-Propenoic acid,3-[3-(acetyloxy)phenyl]-;(2E)-3-[3-(Acetyloxy)phenyl]-2-propenoic acid #

Suppliers and Price of 3-Acetoxycinnamic 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
  • Sigma-Aldrich
  • 3-ACETOXYCINNAMIC ACID Aldrich
  • 250mg
  • $ 57.00
  • Biosynth Carbosynth
  • 3-Acetylcoumaric acid
  • 250 g
  • $ 340.00
  • Biosynth Carbosynth
  • 3-Acetylcoumaric acid
  • 50 g
  • $ 90.00
Total 7 raw suppliers
Chemical Property of 3-Acetoxycinnamic acid
Chemical Property:
  • Vapor Pressure:3.19E-06mmHg at 25°C 
  • Boiling Point:373°C at 760 mmHg 
  • Flash Point:147.8°C 
  • PSA:63.60000 
  • Density:1.267g/cm3 
  • LogP:1.70970 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:206.05790880
  • Heavy Atom Count:15
  • Complexity:270
Purity/Quality:

98%min *data from raw suppliers

3-ACETOXYCINNAMIC ACID Aldrich *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)OC1=CC=CC(=C1)C=CC(=O)O
  • Isomeric SMILES:CC(=O)OC1=CC=CC(=C1)/C=C/C(=O)O
Technology Process of 3-Acetoxycinnamic acid

There total 6 articles about 3-Acetoxycinnamic 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 pyridine; In tetrahydrofuran; at 20 - 30 ℃; for 15h;
Guidance literature:
Multi-step reaction with 3 steps
1: toluene / 4 h / 80 °C
2: sodium hydroxide / methanol / 4 h / 70 °C
3: triethylamine / 2 h / 70 °C
With triethylamine; sodium hydroxide; In methanol; toluene;
DOI:10.3390/molecules16053580
Guidance literature:
Multi-step reaction with 2 steps
1: SnCl2; hydrochloric acid / ueber mehrerer Stufen
2: sodium acetate
With hydrogenchloride; sodium acetate; tin(ll) chloride;
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