Home Other Building Blocks 26305-13-5
26305-13-5,MFCD00010708
Catalog No.:AA002SKS

26305-13-5 | 2,4-Dihydroxy-5,6-dimethylpyrimidine

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1g
97%
in stock  
$14.00   $10.00
- +
25g
97%
in stock  
$136.00   $96.00
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  • 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:
AA002SKS
Chemical Name:
2,4-Dihydroxy-5,6-dimethylpyrimidine
CAS Number:
26305-13-5
Molecular Formula:
C6H8N2O2
Molecular Weight:
140.1399
MDL Number:
MFCD00010708
SMILES:
Cc1[nH]c(=O)[nH]c(=O)c1C
Properties
Properties
 
BP:
408.8°C at 760 mmHg  
Form:
Solid  
MP:
297-300 °C (dec.);(lit.);  
Refractive Index:
1.5065 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
230  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
XLogP3:
-0.2  

Upstream Synthesis Route

[1]Patent:EP3239143,2017,A2,.Locationinpatent:Paragraph0503

[2]Patent:WO2016/22460,2016,A1,.Locationinpatent:Page/Pagecolumn140-141

[3]Patent:WO2017/66428,2017,A1,.Locationinpatent:Page/Pagecolumn253

[4]Patent:WO2013/123401,2013,A1,.Locationinpatent:Page/Pagecolumn40

[5]Nucleosides,NucleotidesandNucleicAcids,2004,vol.23,#11,p.1707-1721

[6]JournalofMedicinalChemistry,2011,vol.54,#2,p.510-524

[7]Molecules,2011,vol.16,#6,p.5113-5129

[8]ChemistryandBiodiversity,2011,vol.8,#8,p.1455-1469

[1]Nucleosides,NucleotidesandNucleicAcids,2011,vol.30,#4,p.293-315

[2]Patent:WO2016/200840,2016,A1,.Locationinpatent:Page/Pagecolumn414

[3]BioorganicandMedicinalChemistryLetters,2010,vol.20,#19,p.5735-5738

[4]Patent:US5750531,1998,A,

[5]Patent:US5750531,1998,A,

[1]Patent:EP1464335,2004,A2,.Locationinpatent:Page/Pagecolumn318

[1]ChemischeBerichte,1901,vol.34,p.2813

[1]Molecules,2011,vol.16,#6,p.5113-5129

[2]ChemistryandBiodiversity,2011,vol.8,#8,p.1455-1469

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1936,vol.58,p.769

[1]JournaloftheAmericanChemicalSociety,1941,vol.63,p.1286,1288

[1]NucleosidesandNucleotides,1994,vol.13,p.177-196

[1]SyntheticCommunications,1991,vol.21,p.2181-2187

26305-13-5    623-48-3    133260-75-0    133260-76-1   
(3-Ethoxycarbonylmethyl-4,5-dimethyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl)-aceticacidethylester 

[1]Heterocycles,1989,vol.28,p.643-652

Literature

Title: Identifying chelators for metalloprotein inhibitors using a fragment-based approach.

Journal: Journal of medicinal chemistry 20110127

Title: The acidity of uracil and uracil analogs in the gas phase: four surprisingly acidic sites and biological implications.

Journal: Journal of the American Society for Mass Spectrometry 20020801

Title: Design, synthesis, and characterization of the antitumor activity of novel ceramide analogues.

Journal: Journal of medicinal chemistry 20011108

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