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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   $19.00
- +
5g
95%
in stock  
$76.00   $54.00
- +
25g
98%
in stock  
$361.00   $253.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
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  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
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

Quotation Request
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SDS
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Tags:6320-15-6 Molecular Formula|6320-15-6 MDL|6320-15-6 SMILES|6320-15-6 6-Chloro-2,4-dimethoxypyrimidine
Catalog No.: AA003L00
6320-15-6,MFCD00006068
6320-15-6 | 6-Chloro-2,4-dimethoxypyrimidine
Pack Size： 250mg
Purity： 98%
in stock
$7.00 $5.00
Pack Size： 1g
Purity： 98%
in stock
$26.00 $19.00
Pack Size： 5g
Purity： 95%
in stock
$76.00 $54.00
Pack Size： 25g
Purity： 98%
in stock
$361.00 $253.00
Quantity
- +
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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
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;  
Complexity: 125  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.8  
Upstream Synthesis Route
6320-15-6    4270-27-3 

[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

6320-15-6    3551-55-1 

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

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

6320-15-6    3289-50-7 

[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

6320-15-6    74-88-4    6972-27-6 

[1]JournaloftheChemicalSociety,1935,p.955

[2]JournaloftheChemicalSociety,1935,p.955

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

6320-15-6    68-12-2    134221-52-6 

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

Downstream Synthesis Route
43212-41-5    124-41-4    6320-15-6 

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

6320-15-6    75-50-3    77767-96-5 

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

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

6320-15-6    74-88-4    6972-27-6 

[1]JournaloftheChemicalSociety,1935,p.955

[2]JournaloftheChemicalSociety,1935,p.955

6320-15-6    4270-27-3 

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

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

[3]Patent:US2628229,1950,

6320-15-6    3551-55-1 

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

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

Literature fold

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 chemistry20100806

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

Journal: The Journal of organic chemistry20080620

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 chemistry20070914

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