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6320-15-6,MFCD00006068
Catalog No.:AA003L00

6320-15-6 | 6-Chloro-2,4-dimethoxypyrimidine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$7.00   $5.00
- +
1g
98%
in stock  
$26.00   $18.00
- +
5g
95%
in stock  
$77.00   $54.00
- +
25g
98%
in stock  
$356.00   $249.00
- +
  • 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:
AA003L00
Chemical Name:
6-Chloro-2,4-dimethoxypyrimidine
CAS Number:
6320-15-6
Molecular Formula:
C6H7ClN2O2
Molecular Weight:
174.5850
MDL Number:
MFCD00006068
SMILES:
COc1cc(Cl)nc(n1)OC
NSC Number:
31796
Properties
Properties
 
BP:
280.6°C at 760 mmHg  
Form:
Solid  
MP:
74-76 °C(lit.)  
Solubility:
Soluble in chloroform, ethyl acetate and methanol.  
Stability:
Hygroscopic  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
125  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Rotatable Bond Count:
2  
XLogP3:
1.8  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1980,vol.102,#15,p.5036-5044

[2]JournalofBiologicalChemistry,1959,vol.234,p.641,643

[3]Patent:US2628229,1950,,

[4]Patent:DE859017,1950,,

[5]Pharmaceuticalbulletin,1957,vol.5,#1,p.28-30

[1]JournalofMolecularCatalysisA:Chemical,2014,vol.393,p.191-209

[2]JournalofOrganicChemistry,1955,vol.20,p.829,833,835

[1]AngewandteChemie-InternationalEdition,2015,vol.54,#12,p.3773-3777

[2]Angew.Chem.,2015,vol.127,#12,p.3844-3848,5

[3]ChemischeBerichte,1959,vol.92,p.583,594

[1]JournaloftheChemicalSociety,1935,p.955

[2]JournaloftheChemicalSociety,1935,p.955

[3]JournaloftheAmericanChemicalSociety,1932,vol.54,p.727,731

[1]JournalofMedicinalChemistry,2007,vol.50,#24,p.6016-6023

Downstream Synthesis Route

[1]ChemischeBerichte,1903,vol.36,p.2234

[1]LiebigsAnnalenderChemie,1981,p.333-341

[2]MonatsheftefurChemie,1956,vol.87,p.131,134

[1]JournaloftheChemicalSociety,1935,p.955

[2]JournaloftheChemicalSociety,1935,p.955

[1]JournaloftheAmericanChemicalSociety,1980,vol.102,p.5036-5044

[2]JournalofBiologicalChemistry,1959,vol.234,p.641,643

[3]Patent:US2628229,1950,

[1]JournalofMolecularCatalysisA:Chemical,2014,vol.393,p.191-209

[2]JournalofOrganicChemistry,1955,vol.20,p.829,833,835

Literature

Title: Short access to 6-substituted pyrimidine derivatives by the S(RN)1 mechanism. Synthesis of 6-substituted uracils through a one-pot procedure.

Journal: The Journal of organic chemistry 20100806

Title: A novel approach to the synthesis of 6-substituted uracils in three-step, one-pot reactions.

Journal: The Journal of organic chemistry 20080620

Title: A new series of 3-alkyl phosphate derivatives of 4,5,6,7-tetrahydro-1-D-ribityl-1H-pyrazolo[3,4-d]pyrimidinedione as inhibitors of lumazine synthase: design, synthesis, and evaluation.

Journal: The Journal of organic chemistry 20070914

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SDS
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