+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Bromides 14529-54-5
14529-54-5,MFCD00464328
Catalog No.:AA001KOT

14529-54-5 | 3,5-Dibromo-1-methylpyridin-2(1H)-one

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$7.00   $5.00
- +
1g
95%
in stock  
$18.00   $13.00
- +
5g
97%
in stock  
$35.00   $25.00
- +
10g
97%
in stock  
$43.00   $30.00
- +
25g
97%
in stock  
$105.00   $74.00
- +
  • 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:
AA001KOT
Chemical Name:
3,5-Dibromo-1-methylpyridin-2(1H)-one
CAS Number:
14529-54-5
Molecular Formula:
C6H5Br2NO
Molecular Weight:
266.9180
MDL Number:
MFCD00464328
SMILES:
Brc1cn(C)c(=O)c(c1)Br
Properties
Properties
 
BP:
259.4°C at 760 mmHg  
Form:
Solid  
MP:
182℃  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
232  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
XLogP3:
1.7  

Upstream Synthesis Route

[1]Synthesis(Germany),2018,vol.50,#17,p.3420-3429

[1]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[2]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[3]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[4]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[5]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[6]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[7]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[8]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[9]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[10]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[1]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[2]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[3]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[4]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[5]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[6]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[7]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[8]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[9]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1982,vol.18,#12,p.1284-1286

[10]KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,#12,p.1662-1664

[1]JustusLiebigsAnnalenderChemie,1931,vol.486,p.71,78

[1]Patent:WO2017/24412,2017,A1,.Locationinpatent:Page/Pagecolumn65

[2]Patent:US2008/153834,2008,A1,.Locationinpatent:Page/Pagecolumn20-21

[3]Patent:WO2008/33858,2008,A2,.Locationinpatent:Page/Pagecolumn127-128

[4]Patent:WO2008/33858,2008,A2,.Locationinpatent:Page/Pagecolumn127-128

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1982,vol.104,p.4142-4146

[2]JournalofOrganicChemistry,1951,vol.16,p.73,79

[1]JustusLiebigsAnnalenderChemie,1931,vol.486,p.71,78

[1]JustusLiebigsAnnalenderChemie,1931,vol.486,p.71,78

[1]ChemistryofHeterocyclicCompounds,1982,vol.18,p.1284-1286    KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,p.1662-1664

[2]ChemistryofHeterocyclicCompounds,1982,vol.18,p.1284-1286    KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,p.1662-1664

[3]ChemistryofHeterocyclicCompounds,1982,vol.18,p.1284-1286    KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,p.1662-1664

[4]ChemistryofHeterocyclicCompounds,1982,vol.18,p.1284-1286    KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,p.1662-1664

[5]ChemistryofHeterocyclicCompounds,1982,vol.18,p.1284-1286    KhimiyaGeterotsiklicheskikhSoedinenii,1982,vol.18,p.1662-1664

[1]Patent:WO2008/33854,2008,A1.Locationinpatent:Page/Pagecolumn63-64

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 14529-54-5
81971-38-2

81971-38-2

 33930-63-1

33930-63-1

 81971-39-3

81971-39-3

 851087-08-6

851087-08-6

 63785-87-5

63785-87-5

 1181458-99-0

1181458-99-0
Building Blocks
More >
Tags:14529-54-5 Molecular Formula|14529-54-5 MDL|14529-54-5 SMILES|14529-54-5 3,5-Dibromo-1-methylpyridin-2(1H)-one