Home Other Building Blocks 14631-20-0
14631-20-0,MFCD00134466
Catalog No.:AA001DTR

14631-20-0 | N4-Acetylcytosine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
10g
95%
in stock  
$8.00   $5.00
- +
500g
98%
in stock  
$77.00   $54.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001DTR
Chemical Name:
N4-Acetylcytosine
CAS Number:
14631-20-0
Molecular Formula:
C6H7N3O2
Molecular Weight:
153.1387
MDL Number:
MFCD00134466
SMILES:
CC(=O)Nc1ccnc(=O)[nH]1
NSC Number:
210403
Properties
Properties
 
Form:
Solid  
MP:
>300 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
255  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
-2.4  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,1991,vol.56,#14,p.4392-4397

[2]JournalofPolymerScience,PartA:PolymerChemistry,2015,vol.53,#9,p.1151-1160

[3]CarbohydrateResearch,1980,vol.78,p.195-204

[4]JournaloftheAmericanChemicalSociety,1990,vol.112,#20,p.7373-7381

[5]AmericanChemicalJournal,1903,vol.29,p.496

[6]AmericanChemicalJournal,1904,vol.31,p.596

[7]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1991,vol.27,#4,p.407-409

[8]KhimiyaGeterotsiklicheskikhSoedinenii,1991,#4,p.512-515

[9]ChemicalResearchinToxicology,1998,vol.11,#9,p.1082-1088

[10]JournaloftheChemicalSociety,1956,p.2388,2392

[11]JournaloftheChemicalSociety,1958,p.3028,3032

[12]BioorganicandMedicinalChemistry,2002,vol.10,#8,p.2671-2680

[13]JournalofPharmacologyandExperimentalTherapeutics,2007,vol.322,#3,p.1023-1035

[14]JournalofChemicalResearch,2007,#5,p.281-283

[15]Patent:WO2010/82128,2010,A1,.Locationinpatent:Page/Pagecolumn18

[16]Patent:US2011/282046,2011,A1,.Locationinpatent:Page/Pagecolumn8

[17]CroaticaChemicaActa,2017,vol.90,#4,p.625-636

[1]CollectionofCzechoslovakChemicalCommunications,1982,vol.47,#11,p.2961-2968

[1]Tetrahedron,1984,vol.40,#1,p.125-135

[1]JournalofOrganicChemistry,1992,vol.57,#12,p.3473-3478

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1991,vol.56,p.4392-4397

[2]JournalofPolymerScience,PartA:PolymerChemistry,2015,vol.53,p.1151-1160

[3]CarbohydrateResearch,1980,vol.78,p.195-204

[4]JournaloftheAmericanChemicalSociety,1990,vol.112,p.7373-7381

[5]AmericanChemicalJournal,1903,vol.29,p.496    AmericanChemicalJournal,1904,vol.31,p.596

[6]ChemicalResearchinToxicology,1998,vol.11,p.1082-1088

[7]JournaloftheChemicalSociety,1956,p.2388,2392    JournaloftheChemicalSociety,1958,p.3028,3032

[8]JournalofPharmacologyandExperimentalTherapeutics,2007,vol.322,p.1023-1035

[9]JournalofChemicalResearch,2007,p.281-283

[10]Patent:WO2010/82128,2010,A1.Locationinpatent:Page/Pagecolumn18

[11]Patent:US2011/282046,2011,A1.Locationinpatent:Page/Pagecolumn8

[12]CroaticaChemicaActa,2017,vol.90,p.625-636

[1]JournalofOrganicChemistry,1992,vol.57,p.3473-3478

[1]Tetrahedron,1999,vol.55,p.1277-1284

[2]NucleosidesandNucleotides,1999,vol.18,p.693-695

14631-20-0    2468-55-5   
1-(1-Pentynyl)-N4-acetylcytosine 

[1]Pelissier,Helene;Rodriguez,Jean;Vollhardt,K.PeterC.[Chemistry-AEuropeanJournal,1999,vol.5,#12,p.3549-3561]

[1]Patent:WO2005/95430,2005,A1.Locationinpatent:Page/Pagecolumn18-20

Literature

Title: Additive Pummerer reaction of 3,5-O-(di-tert-butyl)silylene-4-thiofuranoid glycal: a high-yield and beta-selective entry to 4'-thioribonucleosides.

Journal: The Journal of organic chemistry 20090320

Title: Stereoselective approach to the Z-isomers of methylenecyclopropane analogues of nucleosides: a new synthesis of antiviral synguanol.

Journal: Nucleosides, nucleotides & nucleic acids 20090301

Title: Ab initio study of a biradical radiationless decay channel of the lowest excited electronic state of cytosine and its derivatives.

Journal: The Journal of chemical physics 20050822

Title: Synthesis and antiviral activity of (Z)- and (E)-2,2-[bis(hydroxymethyl)cyclopropylidene]methylpurines and -pyrimidines: second-generation methylenecyclopropane analogues of nucleosides.

Journal: Journal of medicinal chemistry 20040129

Title: Singlet excited-state lifetimes of cytosine derivatives measured by femtosecond transient absorption.

Journal: Photochemistry and photobiology 20030201

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