56059-30-4,MFCD00832183
Catalog No.:AA003MON

56059-30-4 | 5-Fluoro-3,4-dihydro-2,4-dioxo-1(2h)-pyrimidineacetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$90.00   $63.00
- +
1g
97%
in stock  
$175.00   $123.00
- +
5g
97%
in stock  
$576.00   $403.00
- +
10g
97%
in stock  
$964.00   $675.00
- +
25g
97%
in stock  
$1,918.00 $1,343.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003MON
Chemical Name:
5-Fluoro-3,4-dihydro-2,4-dioxo-1(2h)-pyrimidineacetic acid
CAS Number:
56059-30-4
Molecular Formula:
C6H5FN2O4
Molecular Weight:
188.1133
MDL Number:
MFCD00832183
SMILES:
OC(=O)Cn1cc(F)c(=O)[nH]c1=O
Properties
Properties
 
Form:
Solid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
312  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.9  

Upstream Synthesis Route

[1]ChemicalCommunications,2011,vol.47,#38,p.10713-10715

[2]MedicinalChemistryResearch,2007,vol.16,#7-9,p.370-379

[3]Nucleosides,NucleotidesandNucleicAcids,2011,vol.30,#4,p.280-292

[4]ChemicalCommunications,2016,vol.52,#30,p.5254-5257

[5]BioorganicandMedicinalChemistryLetters,2016,vol.26,#11,p.2584-2588

[6]Chemistry-AEuropeanJournal,2013,vol.19,#38,p.12806-12814

[7]Molecules,2017,vol.22,#11,

[8]CarbohydratePolymers,2017,vol.157,p.1442-1450

[9]Patent:WO2017/89800,2017,A1,.Locationinpatent:Page/Pagecolumn37;39

[10]Patent:US2008/4237,2008,A1,.Locationinpatent:Page/Pagecolumn5;9

[11]Patent:US2008/85871,2008,A1,.Locationinpatent:Page/Pagecolumn6-7

[12]ChemistryofNaturalCompounds,1994,vol.30,#5,p.607-612

[13]KhimiyaPrirodnykhSoedinenii,1994,#5,p.655-662

[14]BulletindesSocietesChimiquesBelges,1995,vol.104,#3,p.129-136

[15]Pharmazie,2006,vol.61,#5,p.489-490

[16]Molecules,2010,vol.15,#4,p.2114-2123

[17]JournaloftheBrazilianChemicalSociety,2011,vol.22,#2,p.308-318

[18]NaturalProductResearch,2011,vol.25,#19,p.1817-1826

[19]InternationalJournalofPharmaceutics,2010,vol.388,#1-2,p.95-100

[20]EuropeanJournalofMedicinalChemistry,2012,vol.49,p.48-54

[21]ChineseChemicalLetters,2012,vol.23,#6,p.677-680

[22]CarbohydratePolymers,2012,vol.87,#4,p.2642-2647,6

[23]Patent:US2014/155577,2014,A1,.Locationinpatent:Paragraph0189

[24]SynthesisandReactivityinInorganic,Metal-OrganicandNano-MetalChemistry,2016,vol.46,#5,p.653-658

[25]Patent:CN107892686,2018,A,.Locationinpatent:Paragraph0031-0034

[1]BioorganicandMedicinalChemistry,2011,vol.19,#12,p.3750-3756

[2]MedChemComm,2016,vol.7,#10,p.2016-2019

[3]ResearchonChemicalIntermediates,2012,vol.38,#7,p.1421-1429

[4]Patent:CN104672294,2017,B,.Locationinpatent:Paragraph0033;0034;0035;0037;0038

[5]Pharmazie,2014,vol.69,#4,p.271-276

[6]ChemicalCommunications,2011,vol.47,#5,p.1482-1484

[7]Patent:CN107698521,2018,A,.Locationinpatent:Paragraph0063;0064;0065

[8]JournalofChemicalCrystallography,2008,vol.38,#11,p.807-813

[9]JournalofChemicalResearch,2009,#4,p.261-264

[10]LettersinOrganicChemistry,2013,vol.10,#8,p.594-601

[11]EuropeanJournalofMedicinalChemistry,2017,vol.125,p.1235-1246

[12]MedChemComm,2017,vol.8,#2,p.385-389

[1]MedicinalChemistryResearch,2001,vol.10,#6,p.390-403

[2]Patent:CN105294661,2016,A,.Locationinpatent:Paragraph0037;0038;0039

[3]Heterocycles,1989,vol.28,#2,p.643-652

[1]Patent:CN108558883,2018,A,.Locationinpatent:Paragraph0070;0183;0184

[1]ChemicalCommunications,2011,vol.47,#5,p.1482-1484

Downstream Synthesis Route

[1]CollectionofCzechoslovakChemicalCommunications,1982,vol.47,p.2806-2813

[1]MedicinalChemistryResearch,2001,vol.10,p.390-403

[2]Patent:CN105294661,2016,A.Locationinpatent:Paragraph0037;0038;0039

[3]EuropeanJournalofMedicinalChemistry,2020,vol.185

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

[1]ChemicalCommunications,2011,vol.47,p.10713-10715

[2]Patent:CN109369625,2019,A.Locationinpatent:Paragraph0038-0040

[3]MedicinalChemistryResearch,2007,vol.16,p.370-379

[4]EuropeanJournalofMedicinalChemistry,2020,vol.190

[5]Nucleosides,nucleotidesandnucleicacids,2011,vol.30,p.280-292

[6]ChemicalCommunications,2016,vol.52,p.5254-5257

[7]ChemicalCommunications,2019,vol.55,p.7683-7686

[8]BioorganicandMedicinalChemistryLetters,2016,vol.26,p.2584-2588

[9]Chemistry-AEuropeanJournal,2013,vol.19,p.12806-12814

[10]Molecules,2017,vol.22

[11]CarbohydratePolymers,2017,vol.157,p.1442-1450

[12]Patent:WO2017/89800,2017,A1.Locationinpatent:Page/Pagecolumn37;39

[13]Patent:US2008/4237,2008,A1.Locationinpatent:Page/Pagecolumn5;9

[14]Patent:US2008/85871,2008,A1.Locationinpatent:Page/Pagecolumn6-7

[15]ChemistryofNaturalCompounds,1994,vol.30,p.607-612    KhimiyaPrirodnykhSoedinenii,1994,p.655-662

[16]BulletindesSocietesChimiquesBelges,1995,vol.104,p.129-136

[17]Pharmazie,2006,vol.61,p.489-490

[18]Molecules,2010,vol.15,p.2114-2123

[19]JournaloftheBrazilianChemicalSociety,2011,vol.22,p.308-318

[20]InternationalJournalofPharmaceutics,2010,vol.388,p.95-100

[21]EuropeanJournalofMedicinalChemistry,2012,vol.49,p.48-54

[22]ChineseChemicalLetters,2012,vol.23,p.677-680

[23]CarbohydratePolymers,2012,vol.87,p.2642-2647,6

[24]Patent:US2014/155577,2014,A1.Locationinpatent:Paragraph0189

[25]SynthesisandReactivityinInorganic,Metal-Organic,andNano-MetalChemistry,2016,vol.46,p.653-658

[26]Patent:CN107892686,2018,A.Locationinpatent:Paragraph0031-0034

[27]Patent:US10441607,2019,B1.Locationinpatent:Page/Pagecolumn43

[1]ChemistryofNaturalCompounds,1994,vol.30,p.607-612    KhimiyaPrirodnykhSoedinenii,1994,p.655-662

Literature

Title: Mouse embryonic stem cell adherent cell differentiation and cytotoxicity (ACDC) assay.

Journal: Reproductive toxicology (Elmsford, N.Y.) 20110501

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

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SDS
Related Products of 56059-30-4
Tags:56059-30-4 Molecular Formula|56059-30-4 MDL|56059-30-4 SMILES|56059-30-4 5-Fluoro-3,4-dihydro-2,4-dioxo-1(2h)-pyrimidineacetic acid
Catalog No.: AA003MON
56059-30-4,MFCD00832183
56059-30-4 | 5-Fluoro-3,4-dihydro-2,4-dioxo-1(2h)-pyrimidineacetic acid
Pack Size: 250mg
Purity: 97%
in stock
$90.00 $63.00
Pack Size: 1g
Purity: 97%
in stock
$175.00 $123.00
Pack Size: 5g
Purity: 97%
in stock
$576.00 $403.00
Pack Size: 10g
Purity: 97%
in stock
$964.00 $675.00
Pack Size: 25g
Purity: 97%
in stock
$1,918.00 $1,343.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003MON
Chemical Name: 5-Fluoro-3,4-dihydro-2,4-dioxo-1(2h)-pyrimidineacetic acid
CAS Number: 56059-30-4
Molecular Formula: C6H5FN2O4
Molecular Weight: 188.1133
MDL Number: MFCD00832183
SMILES: OC(=O)Cn1cc(F)c(=O)[nH]c1=O
Properties
Form: Solid  
Storage: Keep in dry area;Room Temperature;  
Complexity: 312  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.9  
Upstream Synthesis Route
51-21-8    79-11-8    56059-30-4 

[1]ChemicalCommunications,2011,vol.47,#38,p.10713-10715

[2]MedicinalChemistryResearch,2007,vol.16,#7-9,p.370-379

[3]Nucleosides,NucleotidesandNucleicAcids,2011,vol.30,#4,p.280-292

[4]ChemicalCommunications,2016,vol.52,#30,p.5254-5257

[5]BioorganicandMedicinalChemistryLetters,2016,vol.26,#11,p.2584-2588

[6]Chemistry-AEuropeanJournal,2013,vol.19,#38,p.12806-12814

[7]Molecules,2017,vol.22,#11,

[8]CarbohydratePolymers,2017,vol.157,p.1442-1450

[9]Patent:WO2017/89800,2017,A1,.Locationinpatent:Page/Pagecolumn37;39

[10]Patent:US2008/4237,2008,A1,.Locationinpatent:Page/Pagecolumn5;9

[11]Patent:US2008/85871,2008,A1,.Locationinpatent:Page/Pagecolumn6-7

[12]ChemistryofNaturalCompounds,1994,vol.30,#5,p.607-612

[13]KhimiyaPrirodnykhSoedinenii,1994,#5,p.655-662

[14]BulletindesSocietesChimiquesBelges,1995,vol.104,#3,p.129-136

[15]Pharmazie,2006,vol.61,#5,p.489-490

[16]Molecules,2010,vol.15,#4,p.2114-2123

[17]JournaloftheBrazilianChemicalSociety,2011,vol.22,#2,p.308-318

[18]NaturalProductResearch,2011,vol.25,#19,p.1817-1826

[19]InternationalJournalofPharmaceutics,2010,vol.388,#1-2,p.95-100

[20]EuropeanJournalofMedicinalChemistry,2012,vol.49,p.48-54

[21]ChineseChemicalLetters,2012,vol.23,#6,p.677-680

[22]CarbohydratePolymers,2012,vol.87,#4,p.2642-2647,6

[23]Patent:US2014/155577,2014,A1,.Locationinpatent:Paragraph0189

[24]SynthesisandReactivityinInorganic,Metal-OrganicandNano-MetalChemistry,2016,vol.46,#5,p.653-658

[25]Patent:CN107892686,2018,A,.Locationinpatent:Paragraph0031-0034

51-21-8    79-08-3    56059-30-4 

[1]BioorganicandMedicinalChemistry,2011,vol.19,#12,p.3750-3756

[2]MedChemComm,2016,vol.7,#10,p.2016-2019

[3]ResearchonChemicalIntermediates,2012,vol.38,#7,p.1421-1429

[4]Patent:CN104672294,2017,B,.Locationinpatent:Paragraph0033;0034;0035;0037;0038

[5]Pharmazie,2014,vol.69,#4,p.271-276

[6]ChemicalCommunications,2011,vol.47,#5,p.1482-1484

[7]Patent:CN107698521,2018,A,.Locationinpatent:Paragraph0063;0064;0065

[8]JournalofChemicalCrystallography,2008,vol.38,#11,p.807-813

[9]JournalofChemicalResearch,2009,#4,p.261-264

[10]LettersinOrganicChemistry,2013,vol.10,#8,p.594-601

[11]EuropeanJournalofMedicinalChemistry,2017,vol.125,p.1235-1246

[12]MedChemComm,2017,vol.8,#2,p.385-389

56059-27-9    56059-30-4 

[1]MedicinalChemistryResearch,2001,vol.10,#6,p.390-403

[2]Patent:CN105294661,2016,A,.Locationinpatent:Paragraph0037;0038;0039

[3]Heterocycles,1989,vol.28,#2,p.643-652

51-21-8    105-36-2    56059-30-4 

[1]Patent:CN108558883,2018,A,.Locationinpatent:Paragraph0070;0183;0184

1273318-25-4    56059-30-4 

[1]ChemicalCommunications,2011,vol.47,#5,p.1482-1484

Downstream Synthesis Route
51-21-8    3926-62-3    84568-51-4    56059-30-4 

[1]CollectionofCzechoslovakChemicalCommunications,1982,vol.47,p.2806-2813

56059-27-9    56059-30-4 

[1]MedicinalChemistryResearch,2001,vol.10,p.390-403

[2]Patent:CN105294661,2016,A.Locationinpatent:Paragraph0037;0038;0039

[3]EuropeanJournalofMedicinalChemistry,2020,vol.185

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

51-21-8    79-11-8    56059-30-4 

[1]ChemicalCommunications,2011,vol.47,p.10713-10715

[2]Patent:CN109369625,2019,A.Locationinpatent:Paragraph0038-0040

[3]MedicinalChemistryResearch,2007,vol.16,p.370-379

[4]EuropeanJournalofMedicinalChemistry,2020,vol.190

[5]Nucleosides,nucleotidesandnucleicacids,2011,vol.30,p.280-292

[6]ChemicalCommunications,2016,vol.52,p.5254-5257

[7]ChemicalCommunications,2019,vol.55,p.7683-7686

[8]BioorganicandMedicinalChemistryLetters,2016,vol.26,p.2584-2588

[9]Chemistry-AEuropeanJournal,2013,vol.19,p.12806-12814

[10]Molecules,2017,vol.22

[11]CarbohydratePolymers,2017,vol.157,p.1442-1450

[12]Patent:WO2017/89800,2017,A1.Locationinpatent:Page/Pagecolumn37;39

[13]Patent:US2008/4237,2008,A1.Locationinpatent:Page/Pagecolumn5;9

[14]Patent:US2008/85871,2008,A1.Locationinpatent:Page/Pagecolumn6-7

[15]ChemistryofNaturalCompounds,1994,vol.30,p.607-612    KhimiyaPrirodnykhSoedinenii,1994,p.655-662

[16]BulletindesSocietesChimiquesBelges,1995,vol.104,p.129-136

[17]Pharmazie,2006,vol.61,p.489-490

[18]Molecules,2010,vol.15,p.2114-2123

[19]JournaloftheBrazilianChemicalSociety,2011,vol.22,p.308-318

[20]InternationalJournalofPharmaceutics,2010,vol.388,p.95-100

[21]EuropeanJournalofMedicinalChemistry,2012,vol.49,p.48-54

[22]ChineseChemicalLetters,2012,vol.23,p.677-680

[23]CarbohydratePolymers,2012,vol.87,p.2642-2647,6

[24]Patent:US2014/155577,2014,A1.Locationinpatent:Paragraph0189

[25]SynthesisandReactivityinInorganic,Metal-Organic,andNano-MetalChemistry,2016,vol.46,p.653-658

[26]Patent:CN107892686,2018,A.Locationinpatent:Paragraph0031-0034

[27]Patent:US10441607,2019,B1.Locationinpatent:Page/Pagecolumn43

658-78-6    56059-30-4    71710-01-5 

[1]ChemistryofNaturalCompounds,1994,vol.30,p.607-612    KhimiyaPrirodnykhSoedinenii,1994,p.655-662

Literature fold

Title: Mouse embryonic stem cell adherent cell differentiation and cytotoxicity (ACDC) assay.

Journal: Reproductive toxicology (Elmsford, N.Y.)20110501

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology20060501

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