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1-Acetylpyrene

Base Information
  • Chemical Name:1-Acetylpyrene
  • CAS No.:3264-21-9
  • Molecular Formula:C18H12O
  • Molecular Weight:244.293
  • Hs Code.:2914399090
  • NSC Number:62422
  • UNII:V74HO8A2YT
  • DSSTox Substance ID:DTXSID10186324
  • Nikkaji Number:J586.199C
  • Wikidata:Q83057578
  • Mol file:3264-21-9.mol
1-Acetylpyrene

Synonyms:1-Acetylpyrene;3264-21-9;1-(Pyren-1-yl)ethanone;1-pyren-1-ylethanone;Ethanone, 1-(1-pyrenyl)-;V74HO8A2YT;NSC-62422;NSC 62422;?1-ACETYLPYRENE;1-Acetylpyrene, 97%;1-(1-Pyrenyl)ethanone;UNII-V74HO8A2YT;1-(1-Pyrenyl)ethanone #;NCIOpen2_002723;SCHEMBL308494;1-(pyren-1-yl)ethan-1-one;LCZC1247;METHYL 1-PYRENYL KETONE;DTXSID10186324;KETONE, METHYL 1-PYRENYL;KCIJNJVCFPSUBQ-UHFFFAOYSA-N;AMY18567;NSC62422;MFCD00021663;AKOS003611281;BS-51095;CS-0204738;FT-0607295;E71338;A821350;J-018807

Suppliers and Price of 1-Acetylpyrene
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
  • Usbiological
  • 1-Acetylpyrene
  • 10g
  • $ 425.00
  • TRC
  • 1-Acetylpyrene
  • 10g
  • $ 140.00
  • Sigma-Aldrich
  • 1-Acetylpyrene 97%
  • 10g
  • $ 184.00
  • Matrix Scientific
  • 1-Acetylpyrene
  • 5g
  • $ 108.00
  • Biosynth Carbosynth
  • 1-Acetylpyrene
  • 25 g
  • $ 262.50
  • Biosynth Carbosynth
  • 1-Acetylpyrene
  • 100 g
  • $ 735.00
  • Biosynth Carbosynth
  • 1-Acetylpyrene
  • 500 g
  • $ 2890.00
  • Biosynth Carbosynth
  • 1-Acetylpyrene
  • 250 g
  • $ 1575.00
  • American Custom Chemicals Corporation
  • 1-ACETYLPYRENE 95.00%
  • 5G
  • $ 861.05
  • Ambeed
  • 1-(Pyren-1-yl)ethanone 98+%
  • 10g
  • $ 200.00
Total 35 raw suppliers
Chemical Property of 1-Acetylpyrene
Chemical Property:
  • Vapor Pressure:7.32E-08mmHg at 25°C 
  • Melting Point:86-89 °C(lit.) 
  • Refractive Index:1.796 
  • Boiling Point:437.7 °C at 760 mmHg 
  • Flash Point:195.6 °C 
  • PSA:17.07000 
  • Density:1.262 g/cm3 
  • LogP:4.78660 
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:244.088815002
  • Heavy Atom Count:19
  • Complexity:374
Purity/Quality:

97% *data from raw suppliers

1-Acetylpyrene *data from reagent suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC(=O)C1=C2C=CC3=CC=CC4=C3C2=C(C=C4)C=C1
  • Uses 1-Acetylpyrene is suitable for use in a comparative study on the photoinitiating efficiency of pyrene, 1-acetylpyrene and 1-(bromoacetyl)pyrene for copolymerization of styrene with acrylonitrile. It may be used in the following studies:As a starting material in the synthesis of ethynlypyrene. 1-(1-chlorovinyl)pyrene was also isolated during this reaction. As a starting material in the synthesis of substituted pyrene derivatives incorporated heterocyclic and sugar moieties.Synthesis of (E)-pyrene oxime ester conjugates of carboxylic acids.Synthesis of tertiary alcohols based on 1-acetylpyrene.Synthesis of (E)-N-[1-(pyren-1-yl)ethylidene]chrysene-2-amine. Synthesis of 3,3-di(methylsulfanyl)-1-(1-pyrenyl)-2-propen-1-one.
Technology Process of 1-Acetylpyrene

There total 18 articles about 1-Acetylpyrene 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 copper(II) sulfate; In methanol; water; for 0.166667h; Inert atmosphere; Photolysis;
DOI:10.1039/c2pp25033k
Guidance literature:
With copper(II) sulfate; In methanol; water; Inert atmosphere; Photolysis;
DOI:10.1039/c2pp25033k
Guidance literature:
With lithium carbonate; In tetrachloromethane; Irradiation;
DOI:10.1021/tx00044a009
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