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636-76-0,MFCD01122318
Catalog No.:AA00EAG3

636-76-0 | 3-Sulfamoylbenzoic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$9.00   $7.00
- +
1g
95%
in stock  
$12.00   $8.00
- +
5g
95%
in stock  
$55.00   $39.00
- +
10g
95%
in stock  
$109.00   $76.00
- +
100g
98%
in stock  
$809.00   $567.00
- +
  • 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:
AA00EAG3
Chemical Name:
3-Sulfamoylbenzoic acid
CAS Number:
636-76-0
Molecular Formula:
C7H7NO4S
Molecular Weight:
201.1998
MDL Number:
MFCD01122318
SMILES:
OC(=O)c1cccc(c1)S(=O)(=O)N
NSC Number:
22977
Properties
Properties
 
BP:
476.1°C at 760 mmHg  
Form:
Solid  
MP:
242 - 243 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
292  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  

Upstream Synthesis Route

[1]Patent:WO2007/23186,2007,A1,.Locationinpatent:Page/Pagecolumn45

[2]EuropeanJournalofMedicinalChemistry,2014,vol.89,p.503-523

[3]JournaloftheAmericanChemicalSociety,2011,vol.133,#40,p.16235-16242

[4]ChemMedChem,2015,vol.10,#9,p.1548-1558

[5]Patent:US2013/35364,2013,A1,.Locationinpatent:Paragraph0233-0235

[6]JournalofMedicinalChemistry,2013,vol.56,#15,p.6146-6155

[7]Fermentforschung,1931,vol.12,p.180,208

[8]JournaloftheChemicalSociety,1921,vol.119,p.1796

[9]BulletindelaSocieteChimiquedeFrance,1945,vol.<5>12,p.954,960

[10]Patent:WO2005/44817,2005,A1,.Locationinpatent:Page/Pagecolumn96

[11]ArchivderPharmazie,2015,vol.348,#6,p.399-407

[1]Patent:EP1679069,2006,A1,.Locationinpatent:Page/Pagecolumn92

[1]JournaloftheChemicalSociety,1921,vol.119,p.1796

[2]EuropeanJournalofMedicinalChemistry,2014,vol.89,p.503-523

[3]ArchivderPharmazie,2015,vol.348,#6,p.399-407

[1]AmericanChemicalJournal,1882,vol.4,p.143

[2]AmericanChemicalJournal,1897,vol.19,p.173,175,189

[3]AmericanChemicalJournal,1882,vol.4,p.143

[4]AmericanChemicalJournal,1886,vol.8,p.187

[1]AmericanChemicalJournal,1897,vol.19,p.173,175,189

Downstream Synthesis Route

[1]JustusLiebigsAnnalenderChemie,1858,vol.106,p.35

[2]JournaloftheChemicalSociety,1945,p.240

[1]AmericanChemicalJournal,1882,vol.4,p.143

[2]AmericanChemicalJournal,1897,vol.19,p.173,175,189

[3]AmericanChemicalJournal,1886,vol.8,p.187

[1]JustusLiebigsAnnalenderChemie,1858,vol.106,p.27

[1]BulletindelaSocieteChimiquedeFrance,1945,vol.<5>12,p.954,960

[1]MedicinalChemistry,2019,vol.15,p.196-206

[2]JustusLiebigsAnnalenderChemie,1858,vol.106,p.35

[3]Patent:EP1679069,2006,A1.Locationinpatent:Page/Pagecolumn92

[4]Patent:US4061761,1977,A

[5]Patent:WO2004/52880,2004,A1.Locationinpatent:Page70

[6]EuropeanJournalofMedicinalChemistry,2018,vol.145,p.606-621

[7]Patent:DE2436263,1976,    Chem.Abstr.,1976,vol.85

[8]Patent:CN108863860,2018,A.Locationinpatent:Paragraph0028;0030;0031

Literature

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

Journal: Bioorganic & medicinal chemistry letters 20101101

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SDS
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