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N4-Benzoylcytosine

Base Information Edit
  • Chemical Name:N4-Benzoylcytosine
  • CAS No.:26661-13-2
  • Molecular Formula:C11H9N3O2
  • Molecular Weight:215.211
  • Hs Code.:29335990
  • European Community (EC) Number:628-907-2
  • NSC Number:211617
  • DSSTox Substance ID:DTXSID00309282
  • Nikkaji Number:J974.010D
  • Wikidata:Q72493915
  • ChEMBL ID:CHEMBL1222779
  • Mol file:26661-13-2.mol
N4-Benzoylcytosine

Synonyms:N4-Benzoylcytosine;26661-13-2;N-(2-oxo-1,2-dihydropyrimidin-4-yl)benzamide;N-Benzoylcytosine;N-(2-oxo-1H-pyrimidin-6-yl)benzamide;Benzamide, N-(1,2-dihydro-2-oxo-4-pyrimidinyl)-;MFCD00239434;NSC 211617;N-(2-Hydroxy-pyrimidin-4-yl)-benzamide;N-(2-Oxo-1,2-dihydro-4-pyrimidinyl)benzamide;N-4-benzoyl cytosine;n-benzoyl cytosine;4-N-benzoylcytosine;N4 -benzoylcytosine;N4-benzoyl cytosine;NSC211617;N4-(Benzoyl)cytosine;N4 -(Benzoyl)cytosine;N4-Benzoylcytosine, 98%;Oprea1_638286;SCHEMBL210467;2-Hydroxy-4-benzamidopyrimidine;CHEMBL1222779;SCHEMBL18549055;SCHEMBL19073177;DTXSID00309282;BCP12250;AKOS015839060;AKOS015888110;AM85688;AS-2052;CCG-308745;CS-W020564;NSC-211617;SB17530;AC-29262;SY036434;B3169;FT-0638627;F14842;N-(2,3-Dihydro-2-oxo-4-pyrimidinyl)benzamide;N-(2-oxo-2,3-dihydropyrimidin-4-yl)benzamide;P15522;A818547;N-(2-Oxo-1,2-dihydro-4-pyrimidinyl)benzamide #;SR-01000463612;SR-01000463612-1;W-202133;F0914-5981

Suppliers and Price of N4-Benzoylcytosine
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
  • Usbiological
  • N4-Benzoylcytosine
  • 100g
  • $ 333.00
  • TRC
  • N4-Benzoylcytosine
  • 100g
  • $ 150.00
  • TCI Chemical
  • N4-Benzoylcytosine >97.0%(HPLC)(T)
  • 5g
  • $ 18.00
  • SynQuest Laboratories
  • N4-Benzoylcytosine
  • 5 g
  • $ 48.00
  • Sigma-Aldrich
  • N4-Benzoylcytosine 98%
  • 10g
  • $ 62.30
  • Matrix Scientific
  • N4-Benzoylcytosine >95%
  • 100g
  • $ 78.00
  • Matrix Scientific
  • N4-Benzoylcytosine >95%
  • 500g
  • $ 245.00
  • Crysdot
  • N-(2-Oxo-1,2-dihydropyrimidin-4-yl)benzamide 97%
  • 100g
  • $ 63.00
  • Chemenu
  • N-(2-oxo-1,2-dihydropyrimidin-4-yl)benzamide 98%
  • 1000g
  • $ 72.00
  • Chemcia Scientific
  • N-(2-Hydroxy-pyrimidin-4-yl)-benzamide >95%
  • 100 G
  • $ 295.00
Total 161 raw suppliers
Chemical Property of N4-Benzoylcytosine Edit
Chemical Property:
  • Vapor Pressure:0Pa at 25℃ 
  • Melting Point:>300 °C (dec.)(lit.) 
  • Refractive Index:1.652 
  • PKA:7.75±0.10(Predicted) 
  • PSA:74.85000 
  • Density:1.33 g/cm3 
  • LogP:1.09520 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C 
  • Solubility.:Aqueous Acid (Slightly, Heated), DMSO+DCl (Slightly, Heated) 
  • XLogP3:0.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:215.069476538
  • Heavy Atom Count:16
  • Complexity:354
Purity/Quality:

98%min. *data from raw suppliers

N4-Benzoylcytosine *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 20/22-36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=O)NC2=CC=NC(=O)N2
  • Uses N4-Benzoylcytosine may be employed for the following syntheses: 3′-C-ethynyl and 3′-C-(1,4-disubstituted-1,2,3-triazolo) double-headed pyranonucleosides 2′-C-methyl-4′-thiocytidine, via the Pummerer reaction2′-fluorinated L-nucleoside analogs N4-Benzoylcytosine is a reactant in the synthesis of 1'',2''-cyclopentyl nucleosides as potential antiviral agents.
Technology Process of N4-Benzoylcytosine

There total 6 articles about N4-Benzoylcytosine 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 dmap; In acetonitrile; for 7h; Heating;
Guidance literature:
In pyridine; methanol;
Guidance literature:
With triethylamine; In acetonitrile; Ambient temperature;
DOI:10.1135/cccc19822786
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