38324-83-3,MFCD08236864
Catalog No.:AA00BYEL

38324-83-3 | 2-Oxo-1,2-dihydropyrimidine-5-carboxylic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$98.00   $69.00
- +
5g
95%
in stock  
$477.00 $334.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00BYEL
Chemical Name:
2-Oxo-1,2-dihydropyrimidine-5-carboxylic acid
CAS Number:
38324-83-3
Molecular Formula:
C5H4N2O3
Molecular Weight:
140.0969
MDL Number:
MFCD08236864
SMILES:
Oc1ncc(cn1)C(=O)O
Properties
Properties
 
Form:
Solid  
MP:
>200°C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
241  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1  

Upstream Synthesis Route

[1]Journalofmedicinalchemistry,2000,vol.43,#21,p.3995-4004

Downstream Synthesis Route

[1]Arukwe,Joseph;Undheim,Kjell[ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1986,vol.40,#9,p.764-767]

[1]Journalofmedicinalchemistry,2000,vol.43,p.3995-4004

[2]Patent:US2009/105266,2009,A1.Locationinpatent:Page/Pagecolumn30

[3]Patent:US2009/105266,2009,A1.Locationinpatent:Page/Pagecolumn30

[1]Journalofmedicinalchemistry,2000,vol.43,p.3995-4004

38324-83-3   
2-chloro-pyrimidine-5-carboxylicacid(3,5-bis-trifluoromethyl-phenyl)-amide 

[1]Journalofmedicinalchemistry,2000,vol.43,p.3995-4004

38324-83-3   
2-bromopyrimidine-5-carboxylicacid 

[1]Patent:WO2008/128968,2008,A1.Locationinpatent:Page/Pagecolumn68;69

Literature

Title: Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement.

Journal: Organic & biomolecular chemistry 20080521

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Tags:38324-83-3 Molecular Formula|38324-83-3 MDL|38324-83-3 SMILES|38324-83-3 2-Oxo-1,2-dihydropyrimidine-5-carboxylic acid
Catalog No.: AA00BYEL
38324-83-3,MFCD08236864
38324-83-3 | 2-Oxo-1,2-dihydropyrimidine-5-carboxylic acid
Pack Size: 1g
Purity: 95%
in stock
$98.00 $69.00
Pack Size: 5g
Purity: 95%
in stock
$477.00 $334.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00BYEL
Chemical Name: 2-Oxo-1,2-dihydropyrimidine-5-carboxylic acid
CAS Number: 38324-83-3
Molecular Formula: C5H4N2O3
Molecular Weight: 140.0969
MDL Number: MFCD08236864
SMILES: Oc1ncc(cn1)C(=O)O
Properties
Form: Solid  
MP: >200°C  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 241  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1  
Upstream Synthesis Route
73781-88-1    38324-83-3 

[1]Journalofmedicinalchemistry,2000,vol.43,#21,p.3995-4004

Downstream Synthesis Route
38324-83-3    110099-99-5 

[1]Arukwe,Joseph;Undheim,Kjell[ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1986,vol.40,#9,p.764-767]

38324-83-3    110099-99-5 

[1]Journalofmedicinalchemistry,2000,vol.43,p.3995-4004

[2]Patent:US2009/105266,2009,A1.Locationinpatent:Page/Pagecolumn30

[3]Patent:US2009/105266,2009,A1.Locationinpatent:Page/Pagecolumn30

73781-88-1    38324-83-3 

[1]Journalofmedicinalchemistry,2000,vol.43,p.3995-4004

38324-83-3   
2-chloro-pyrimidine-5-carboxylicacid(3,5-bis-trifluoromethyl-phenyl)-amide 

[1]Journalofmedicinalchemistry,2000,vol.43,p.3995-4004

38324-83-3   
2-bromopyrimidine-5-carboxylicacid 

[1]Patent:WO2008/128968,2008,A1.Locationinpatent:Page/Pagecolumn68;69

Literature fold

Title: Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement.

Journal: Organic & biomolecular chemistry20080521

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