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69716-28-5,MFCD20257786
Catalog No.:AA005UMY

69716-28-5 | N-Hydroxypicolinimidoyl chloride

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250mg
95%
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$28.00   $20.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
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  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA005UMY
Chemical Name:
N-Hydroxypicolinimidoyl chloride
CAS Number:
69716-28-5
Molecular Formula:
C6H5ClN2O
Molecular Weight:
156.5697
MDL Number:
MFCD20257786
SMILES:
O/N=C(/c1ccccn1)\Cl
Properties
Properties
 
Form:
Solid  
MP:
144℃ (benzene )  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
138  
Covalently-Bonded Unit Count:
1  
Defined Bond Stereocenter Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2  

Upstream Synthesis Route

[1]Patent:WO2018/64119,2018,A1,.Locationinpatent:Paragraph1352

[2]Patent:WO2008/23248,2008,A2,.Locationinpatent:Page/Pagecolumn94

[3]Patent:US2009/247478,2009,A1,.Locationinpatent:Page/Pagecolumn50

[4]Patent:WO2012/76989,2012,A1,.Locationinpatent:Page/Pagecolumn52

[5]Tetrahedron,2000,vol.56,#8,p.1057-1064

[6]JournaloftheChineseChemicalSociety,2007,vol.54,#3,p.643-652

[7]AustralianJournalofChemistry,2010,vol.63,#3,p.445-451

[8]Tetrahedron,2012,vol.68,#30,p.6018-6031

[9]ChemMedChem,2013,vol.8,#7,p.1210-1223

[10]AngewandteChemie-InternationalEdition,2016,vol.55,#12,p.3997-4001

[11]Angew.Chem.,2016,vol.128,#12,p.4065-4069,5

[12]BioorganicandMedicinalChemistry,2017,vol.25,#20,p.5290-5302

[1]Patent:WO2011/17578,2011,A1,.Locationinpatent:Page/Pagecolumn80

[2]Patent:WO2010/85582,2010,A1,.Locationinpatent:Page/Pagecolumn42-43

[1]SyntheticCommunications,1988,vol.18,#12,p.1427-1432

[2]JournalofHeterocyclicChemistry,2009,vol.46,#6,p.1271-1279

[3]Phosphorus,SulfurandSiliconandtheRelatedElements,2005,vol.180,#12,p.2653-2666

[1]ChemMedChem,2013,vol.8,#7,p.1210-1223

[2]AngewandteChemie-InternationalEdition,2016,vol.55,#12,p.3997-4001

[3]Angew.Chem.,2016,vol.128,#12,p.4065-4069,5

[4]BioorganicandMedicinalChemistry,2017,vol.25,#20,p.5290-5302

[5]Patent:WO2018/64119,2018,A1,

[1]TetrahedronLetters,1995,vol.36,#2,p.327-330

Downstream Synthesis Route

[1]Pharmazie,1986,vol.41,p.699-702

[1]BulletindesSocietesChimiquesBelges,1987,vol.96,p.675-710

[1]SyntheticCommunications,1988,vol.18,p.1427-1432

[2]JournalofHeterocyclicChemistry,2009,vol.46,p.1271-1279

[3]Phosphorus,SulfurandSiliconandtheRelatedElements,2005,vol.180,p.2653-2666

13676-54-5    69716-28-5   
C33H22N6O6 

[1]CollectionofCzechoslovakChemicalCommunications,1992,vol.57,p.1982-1992

[1]Pharmazie,1986,vol.41,p.699-702

Literature
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