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Paprazine

Base Information Edit
  • Chemical Name:Paprazine
  • CAS No.:36417-86-4
  • Molecular Formula:C17H17NO3
  • Molecular Weight:283.327
  • Hs Code.:
  • NSC Number:719214
  • UNII:5WQM3PJ2UK
  • DSSTox Substance ID:DTXSID401318618
  • Nikkaji Number:J431.372K,J109.849G
  • Wikidata:Q27134147
  • Metabolomics Workbench ID:48560
  • ChEMBL ID:CHEMBL64286
  • Mol file:36417-86-4.mol
Paprazine

Synonyms:N-p-trans-Coumaroyltyramine;36417-86-4;Paprazine;p-coumaroyltyramine;N-P-Coumaroyltyramine;N-trans-Coumaroyltyramine;4-coumaroyltyramine;trans-N-(p-coumaroyl)tyramine;5WQM3PJ2UK;N-P-Coumaroyl Tyramine;(E)-N-(4-Hydroxyphenethyl)-3-(4-hydroxyphenyl)acrylamide;UNII-5WQM3PJ2UK;(E)-3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide;trans-n-p-coumaroyl tyramine;CHEMBL64286;CHEBI:65665;2-Propenamide, 3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-;(2E)-3-(4-Hydroxyphenyl)-N-(2-(4-hydroxyphenyl)ethyl)-2-propenamide;(2E)-3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide;N-(p-Hydroxyphenyl)ethyl p-hydroxycinnamide;20375-37-5;n-(4-hydroxyphenethyl)-4-hydroxybenzeneacrylamide;n-coumaroyltyramine;MFCD20260399;Coumaroyl tyramine;NSC719214;N-p-coumaroyl-tyramine;n trans p coumaroyltyramine;N-trans-p-coumaroyltyramine;Trans-N-Hydroxycinnamoyltyramine;SCHEMBL19551426;ACon1_001913;DTXSID401318618;BDBM50069772;AKOS016814940;NSC-719214;NCGC00180009-01;F17680;BRD-K84677622-001-01-5;Q27134147;Z1690788261;(2E)-3-(4-Hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-2-propenamide #;(2e)-3-(4-hydroxyphenyl)-n-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide;(E)-3-(4-Hydroxy-phenyl)-N-[2-(4-hydroxy-phenyl)-ethyl]-acrylamide;2-Propenamide, 3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-, (2E)-;111129-11-4

Suppliers and Price of Paprazine
Supply Marketing:Edit
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
  • Crysdot
  • N-p-Coumaroyltyramine 95+%
  • 5mg
  • $ 300.00
  • Crysdot
  • N-p-Coumaroyltyramine 95+%
  • 10mg
  • $ 460.00
  • ChemScene
  • N-p-trans-Coumaroyltyramine 98.78%
  • 5mg
  • $ 336.00
  • ChemScene
  • N-p-trans-Coumaroyltyramine 98.78%
  • 10mg
  • $ 571.00
  • AvaChem
  • Paprazine
  • 10mg
  • $ 490.00
  • AvaChem
  • Paprazine
  • 5mg
  • $ 290.00
  • AvaChem
  • Paprazine
  • 20mg
  • $ 690.00
  • AvaChem
  • Paprazine
  • 1mg
  • $ 119.00
  • Arctom
  • (E)-N-(4-Hydroxyphenethyl)-3-(4-hydroxyphenyl)acrylamide
  • 1g
  • $ 895.00
  • Arctom
  • N-p-trans-Coumaroyltyramine
  • 10mg
  • $ 268.00
Total 32 raw suppliers
Chemical Property of Paprazine Edit
Chemical Property:
  • Boiling Point:586.5 °C at 760 mmHg 
  • Flash Point:308.5 °C 
  • PSA:69.56000 
  • Density:1.248 g/cm3 
  • LogP:2.86080 
  • Storage Temp.:2-8°C 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:283.12084340
  • Heavy Atom Count:21
  • Complexity:340
Purity/Quality:

98%min *data from raw suppliers

N-p-Coumaroyltyramine 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O
  • Isomeric SMILES:C1=CC(=CC=C1CCNC(=O)/C=C/C2=CC=C(C=C2)O)O
Technology Process of Paprazine

There total 6 articles about Paprazine 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 tetrabutylammomium bromide; palladium diacetate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 130 - 140 ℃; Microwave irradiation; Continuous-flow conditions;
DOI:10.1002/chem.201002102
Guidance literature:
With sodium hydrogencarbonate; In water; acetone; for 24h;
DOI:10.1016/0031-9422(96)00173-2
Guidance literature:
With sodium carbonate; In ethanol; for 2h; Yield given; Heating;
DOI:10.1248/cpb.40.396
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