1083326-75-3,MFCD12964555
Catalog No.:AA008XD2

1083326-75-3 | N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$85.00   $60.00
- +
250mg
95%
in stock  
$147.00   $103.00
- +
1g
95%
in stock  
$389.00   $272.00
- +
5g
97%
in stock  
$1,680.00 $1,176.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA008XD2
Chemical Name:
N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide
CAS Number:
1083326-75-3
Molecular Formula:
C13H21BN2O5S
Molecular Weight:
328.1922
MDL Number:
MFCD12964555
SMILES:
COc1ncc(cc1NS(=O)(=O)C)B1OC(C(O1)(C)C)(C)C
Properties
Computed Properties
 
Complexity:
489  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Upstream Synthesis Route

[1]OrganicProcessResearchandDevelopment,2018,vol.22,#3,p.368-376

[2]Patent:US2014/134133,2014,A1,.Locationinpatent:Paragraph0441

[3]BioorganicandMedicinalChemistry,2018,vol.26,#3,p.637-646

[4]JournalofMedicinalChemistry,2018,vol.61,#14,p.6087-6109

[5]EuropeanJournalofMedicinalChemistry,2018,vol.146,p.460-470

[6]BioorganicandMedicinalChemistry,2018,vol.26,#8,p.1675-1685

[7]Patent:WO2012/32067,2012,A1,.Locationinpatent:Page/Pagecolumn61

[8]Patent:WO2014/28968,2014,A1,.Locationinpatent:Page/Pagecolumn87;88

[9]Patent:US9326987,2016,B2,.Locationinpatent:Page/Pagecolumn166;167

[10]Patent:CN106674200,2017,A,.Locationinpatent:Paragraph0096;0097

[1]JournalofMedicinalChemistry,2015,vol.58,#18,p.7381-7399

[2]Patent:WO2010/102958,2010,A1,.Locationinpatent:Page/Pagecolumn98;99

[3]Patent:WO2011/67365,2011,A1,.Locationinpatent:Page/Pagecolumn69

[4]Patent:WO2012/32067,2012,A1,.Locationinpatent:Page/Pagecolumn55

[5]Patent:WO2014/60432,2014,A1,.Locationinpatent:Page/Pagecolumn130

[6]Patent:US9326987,2016,B2,.Locationinpatent:Page/Pagecolumn95;133

[7]Patent:WO2009/147187,2009,A1,.Locationinpatent:Page/Pagecolumn114

[8]Patent:WO2010/125082,2010,A1,.Locationinpatent:Page/Pagecolumn75

[1]Patent:WO2011/67365,2011,A1,

[2]Patent:WO2012/32067,2012,A1,

[3]Patent:WO2012/32067,2012,A1,

[4]Patent:WO2014/28968,2014,A1,

[5]Patent:US2014/134133,2014,A1,

[6]Patent:US9326987,2016,B2,

[7]Patent:US9326987,2016,B2,

[8]BioorganicandMedicinalChemistry,2018,vol.26,#3,p.637-646

[9]EuropeanJournalofMedicinalChemistry,2018,vol.146,p.460-470

[10]BioorganicandMedicinalChemistry,2018,vol.26,#8,p.1675-1685

[11]JournalofMedicinalChemistry,2018,vol.61,#14,p.6087-6109

[12]Patent:WO2009/147187,2009,A1,

[13]Patent:WO2010/125082,2010,A1,

[1]Patent:WO2014/60431,2014,A1,.Locationinpatent:Page/Pagecolumn85-86

[1]Patent:WO2011/67365,2011,A1,

[2]Patent:WO2012/32067,2012,A1,

[3]Patent:WO2014/60431,2014,A1,

[4]Patent:US9326987,2016,B2,

[5]Patent:WO2009/147187,2009,A1,

[6]Patent:WO2010/125082,2010,A1,

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,2015,vol.58,p.7381-7399

[2]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn98;99

[3]Patent:WO2011/67365,2011,A1.Locationinpatent:Page/Pagecolumn69

[4]Patent:WO2012/32067,2012,A1.Locationinpatent:Page/Pagecolumn55

[5]Patent:WO2014/60432,2014,A1.Locationinpatent:Page/Pagecolumn130

[6]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn95;133

[7]Patent:WO2009/147187,2009,A1.Locationinpatent:Page/Pagecolumn114

[8]Patent:WO2010/125082,2010,A1.Locationinpatent:Page/Pagecolumn75

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn148;149

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn192;193

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn156;157;158

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn199;200

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn115;116

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn112;113

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn151;152

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn194;195

Literature
Quotation Request
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Additional Info:
SDS
Related Products of 1083326-75-3
Tags:1083326-75-3 Molecular Formula|1083326-75-3 MDL|1083326-75-3 SMILES|1083326-75-3 N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide
Catalog No.: AA008XD2
1083326-75-3,MFCD12964555
1083326-75-3 | N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide
Pack Size: 100mg
Purity: 95%
in stock
$85.00 $60.00
Pack Size: 250mg
Purity: 95%
in stock
$147.00 $103.00
Pack Size: 1g
Purity: 95%
in stock
$389.00 $272.00
Pack Size: 5g
Purity: 97%
in stock
$1,680.00 $1,176.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA008XD2
Chemical Name: N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide
CAS Number: 1083326-75-3
Molecular Formula: C13H21BN2O5S
Molecular Weight: 328.1922
MDL Number: MFCD12964555
SMILES: COc1ncc(cc1NS(=O)(=O)C)B1OC(C(O1)(C)C)(C)C
Properties
Complexity: 489  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Upstream Synthesis Route
1083327-58-5    73183-34-3    1083326-75-3 

[1]OrganicProcessResearchandDevelopment,2018,vol.22,#3,p.368-376

[2]Patent:US2014/134133,2014,A1,.Locationinpatent:Paragraph0441

[3]BioorganicandMedicinalChemistry,2018,vol.26,#3,p.637-646

[4]JournalofMedicinalChemistry,2018,vol.61,#14,p.6087-6109

[5]EuropeanJournalofMedicinalChemistry,2018,vol.146,p.460-470

[6]BioorganicandMedicinalChemistry,2018,vol.26,#8,p.1675-1685

[7]Patent:WO2012/32067,2012,A1,.Locationinpatent:Page/Pagecolumn61

[8]Patent:WO2014/28968,2014,A1,.Locationinpatent:Page/Pagecolumn87;88

[9]Patent:US9326987,2016,B2,.Locationinpatent:Page/Pagecolumn166;167

[10]Patent:CN106674200,2017,A,.Locationinpatent:Paragraph0096;0097

893440-50-1    124-63-0    1083326-75-3 

[1]JournalofMedicinalChemistry,2015,vol.58,#18,p.7381-7399

[2]Patent:WO2010/102958,2010,A1,.Locationinpatent:Page/Pagecolumn98;99

[3]Patent:WO2011/67365,2011,A1,.Locationinpatent:Page/Pagecolumn69

[4]Patent:WO2012/32067,2012,A1,.Locationinpatent:Page/Pagecolumn55

[5]Patent:WO2014/60432,2014,A1,.Locationinpatent:Page/Pagecolumn130

[6]Patent:US9326987,2016,B2,.Locationinpatent:Page/Pagecolumn95;133

[7]Patent:WO2009/147187,2009,A1,.Locationinpatent:Page/Pagecolumn114

[8]Patent:WO2010/125082,2010,A1,.Locationinpatent:Page/Pagecolumn75

884495-39-0    1083326-75-3 

[1]Patent:WO2011/67365,2011,A1,

[2]Patent:WO2012/32067,2012,A1,

[3]Patent:WO2012/32067,2012,A1,

[4]Patent:WO2014/28968,2014,A1,

[5]Patent:US2014/134133,2014,A1,

[6]Patent:US9326987,2016,B2,

[7]Patent:US9326987,2016,B2,

[8]BioorganicandMedicinalChemistry,2018,vol.26,#3,p.637-646

[9]EuropeanJournalofMedicinalChemistry,2018,vol.146,p.460-470

[10]BioorganicandMedicinalChemistry,2018,vol.26,#8,p.1675-1685

[11]JournalofMedicinalChemistry,2018,vol.61,#14,p.6087-6109

[12]Patent:WO2009/147187,2009,A1,

[13]Patent:WO2010/125082,2010,A1,

893440-50-1    124-63-0    1083326-75-3 

[1]Patent:WO2014/60431,2014,A1,.Locationinpatent:Page/Pagecolumn85-86

73183-34-3    1083326-75-3 

[1]Patent:WO2011/67365,2011,A1,

[2]Patent:WO2012/32067,2012,A1,

[3]Patent:WO2014/60431,2014,A1,

[4]Patent:US9326987,2016,B2,

[5]Patent:WO2009/147187,2009,A1,

[6]Patent:WO2010/125082,2010,A1,

Downstream Synthesis Route
893440-50-1    124-63-0    1083326-75-3 

[1]JournalofMedicinalChemistry,2015,vol.58,p.7381-7399

[2]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn98;99

[3]Patent:WO2011/67365,2011,A1.Locationinpatent:Page/Pagecolumn69

[4]Patent:WO2012/32067,2012,A1.Locationinpatent:Page/Pagecolumn55

[5]Patent:WO2014/60432,2014,A1.Locationinpatent:Page/Pagecolumn130

[6]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn95;133

[7]Patent:WO2009/147187,2009,A1.Locationinpatent:Page/Pagecolumn114

[8]Patent:WO2010/125082,2010,A1.Locationinpatent:Page/Pagecolumn75

1083326-75-3    1245465-34-2    1245466-41-4 

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn148;149

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn192;193

1083326-75-3    1245465-37-5    1245466-45-8 

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn156;157;158

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn199;200

1083326-75-3    1245465-38-6    1245465-47-7 

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn115;116

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn112;113

1083326-75-3    1245465-40-0    1245465-88-6 

[1]Patent:WO2010/102958,2010,A1.Locationinpatent:Page/Pagecolumn151;152

[2]Patent:US9326987,2016,B2.Locationinpatent:Page/Pagecolumn194;195

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