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3-{[1,1'-Biphenyl]-3-YL}prop-2-enoic acid

Base Information
  • Chemical Name:3-{[1,1'-Biphenyl]-3-YL}prop-2-enoic acid
  • CAS No.:60521-26-8
  • Molecular Formula:C15H12O2
  • Molecular Weight:224.259
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40696446
  • Mol file:60521-26-8.mol
3-{[1,1'-Biphenyl]-3-YL}prop-2-enoic acid

Synonyms:3-{[1,1'-BIPHENYL]-3-YL}PROP-2-ENOIC ACID;3-([1,1'-Biphenyl]-3-yl)prop-2-enoic acid;3-phenylcinnamic acid;DTXSID40696446;QQQNPVHFBDPNNA-UHFFFAOYSA-N;AKOS030239320;(E)-3-([1,1'-biphenyl]-3-yl)acrylic acid

Suppliers and Price of 3-{[1,1'-Biphenyl]-3-YL}prop-2-enoic 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
  • TRC
  • 3-([1,1''-Biphenyl]-3-yl)acrylicAcid
  • 50mg
  • $ 90.00
  • Crysdot
  • 3-([1,1'-Biphenyl]-3-yl)acrylicacid 95+%
  • 1g
  • $ 772.00
  • Alichem
  • 3-([1,1'-Biphenyl]-3-yl)acrylicacid
  • 1g
  • $ 634.28
Total 30 raw suppliers
Chemical Property of 3-{[1,1'-Biphenyl]-3-YL}prop-2-enoic acid
Chemical Property:
  • Boiling Point:424.1±24.0 °C at 760 mmHg 
  • Flash Point:317.7±13.8 °C 
  • PSA:37.30000 
  • Density:1.2±0.1 g/cm3 
  • LogP:3.45140 
  • Storage Temp.:2-8°C 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:224.083729621
  • Heavy Atom Count:17
  • Complexity:277
Purity/Quality:

97% *data from raw suppliers

3-([1,1''-Biphenyl]-3-yl)acrylicAcid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C2=CC=CC(=C2)C=CC(=O)O
  • Use Description (E)-3-Phenylcinnamic acid, a specific chemical compound, serves distinct functions across various fields. In the pharmaceutical sector, it plays a pivotal role as a key intermediate in the synthesis of pharmaceutical compounds, contributing to drug discovery and the development of molecules with potential therapeutic applications. In organic synthesis, (E)-3-phenylcinnaMic acid acts as a versatile building block, enabling the creation of complex molecular structures for research and practical applications. Additionally, in the field of natural product chemistry, it may be explored for its potential contributions to the synthesis of naturally occurring compounds with biological activities. Its applications in pharmaceuticals, organic synthesis, and natural product chemistry underscore its significance in driving innovation, scientific exploration, and potential medical breakthroughs across these different domains.
Technology Process of 3-{[1,1'-Biphenyl]-3-YL}prop-2-enoic acid

There total 8 articles about 3-{[1,1'-Biphenyl]-3-YL}prop-2-enoic 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 piperidine; In pyridine; for 2h; Heating;
DOI:10.1002/ardp.200400886
Guidance literature:
With sodium hydroxide; potassium carbonate; tetrakis(triphenylphosphine)palladium (0); In methanol; ethanol; toluene;
Guidance literature:
Multi-step reaction with 2 steps
1: 86 percent / aq. K2CO3 / tetrakis(triphenylphosphine)palladium(0); [1,1'-bis(diphenylphosphine)ferrocene]palladium(II) chloride / toluene; ethanol / 5 h / Heating
2: 91 percent / piperidine / pyridine / 2 h / Heating
With piperidine; potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium(0); In pyridine; ethanol; toluene; 1: Suzuki coupling / 2: Knoevenagel condensation;
DOI:10.1002/ardp.200400886
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