Home Amines 22094-62-8
22094-62-8,MFCD00115506
Catalog No.:AA0039HM

22094-62-8 | 6-Aminobenzo[d]isothiazol-3(2H)-one 1,1-dioxide

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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
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  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0039HM
Chemical Name:
6-Aminobenzo[d]isothiazol-3(2H)-one 1,1-dioxide
CAS Number:
22094-62-8
Molecular Formula:
C7H6N2O3S
Molecular Weight:
198.1991
MDL Number:
MFCD00115506
SMILES:
Nc1ccc2c(c1)S(=O)(=O)NC2=O
Properties
Computed Properties
 
Complexity:
332  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
XLogP3:
0.2  

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistry,2014,vol.22,p.1529-1538

[2]AsianJournalofChemistry,2017,vol.29,p.1622-1624

[3]BioorganicandMedicinalChemistry,2012,vol.20,p.2811-2821

[4]Patent:WO2012/48222,2012,A1.Locationinpatent:Page/Pagecolumn98-99

[5]BulletinoftheChemicalSocietyofJapan,1982,vol.55,p.3824-3827

[6]Patent:WO2008/24634,2008,A1.Locationinpatent:Page/Pagecolumn168

[7]JournalofEnzymeInhibitionandMedicinalChemistry,2014,vol.29,p.118-123

[1]BulletinoftheChemicalSocietyofJapan,1982,vol.55,p.3824-3827

[2]Patent:WO2012/48222,2012,A1

[3]BioorganicandMedicinalChemistry,2012,vol.20,p.2811-2821

[4]JournalofEnzymeInhibitionandMedicinalChemistry,2014,vol.29,p.118-123

[5]BioorganicandMedicinalChemistry,2014,vol.22,p.1529-1538

[6]AsianJournalofChemistry,2017,vol.29,p.1622-1624

[1]Kamogawa;Yamamoto;Nanasawa[BulletinoftheChemicalSocietyofJapan,1982,vol.55,#12,p.3824-3827]

[2]CurrentPatentAssignee:ABBVIEINC-WO2012/48222,2012,A1

[3]Gener,Nahit;Demir,Dudu;Sonmez,Fatih;Kucukislamoglu,Mustafa[BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2811-2821]

[4]Sonmez,Fatih;Bilen,Cigdem;Sumersan,Sinem;Gencer,Nahit;Isik,Semra;Arslan,Oktay;Kucukislamoglu,Mustafa[JournalofEnzymeInhibitionandMedicinalChemistry,2014,vol.29,#1,p.118-123]

[1]Locationinpatent:experimentalpartGener,Nahit;Demir,Dudu;Sonmez,Fatih;Kucukislamoglu,Mustafa[BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2811-2821]

[2]Sonmez,Fatih;Bilen,Cigdem;Sumersan,Sinem;Gencer,Nahit;Isik,Semra;Arslan,Oktay;Kucukislamoglu,Mustafa[JournalofEnzymeInhibitionandMedicinalChemistry,2014,vol.29,#1,p.118-123]

[1]Locationinpatent:experimentalpartGener,Nahit;Demir,Dudu;Sonmez,Fatih;Kucukislamoglu,Mustafa[BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2811-2821]

[2]Sonmez,Fatih;Bilen,Cigdem;Sumersan,Sinem;Gencer,Nahit;Isik,Semra;Arslan,Oktay;Kucukislamoglu,Mustafa[JournalofEnzymeInhibitionandMedicinalChemistry,2014,vol.29,#1,p.118-123]

Literature

Title: New saccharin derivatives as tyrosinase inhibitors.

Journal: Bioorganic & medicinal chemistry 20120501

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SDS
Tags:22094-62-8 Molecular Formula|22094-62-8 MDL|22094-62-8 SMILES|22094-62-8 6-Aminobenzo[d]isothiazol-3(2H)-one 1,1-dioxide