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Home Sulfos 4-Amino-n-phenyl-benzenesulfonamide

4-Amino-n-phenyl-benzenesulfonamide

CAS No.:
127-77-5
Catalog Number:
AG000WJM
Molecular Formula:
C12H12N2O2S
Molecular Weight:
248.3009
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$124
- +
5g
98%
In Stock USA
United States
$375
- +
10g
98%
In Stock USA
United States
$563
- +
25g
98%
In Stock USA
United States
$1125
- +
Product Description
Catalog Number:
AG000WJM
Chemical Name:
4-Amino-n-phenyl-benzenesulfonamide
CAS Number:
127-77-5
Molecular Formula:
C12H12N2O2S
Molecular Weight:
248.3009
MDL Number:
MFCD00233654
IUPAC Name:
4-amino-N-phenylbenzenesulfonamide
InChI:
InChI=1S/C12H12N2O2S/c13-10-6-8-12(9-7-10)17(15,16)14-11-4-2-1-3-5-11/h1-9,14H,13H2
InChI Key:
YBUXKQSCKVQATK-UHFFFAOYSA-N
SMILES:
Nc1ccc(cc1)S(=O)(=O)Nc1ccccc1
EC Number:
204-865-7
UNII:
2Y70F6K03F
NSC Number:
2619
Properties
Complexity:
323  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
248.062g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
248.3g/mol
Monoisotopic Mass:
248.062g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
80.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.6  
Literature
Title Journal
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Design and synthesis of benzenesulfonanilides active against methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus. Bioorganic & medicinal chemistry 20080601
Analgesic agents without gastric damage: design and synthesis of structurally simple benzenesulfonanilide-type cyclooxygenase-1-selective inhibitors. Bioorganic & medicinal chemistry 20070115
Identification of a class of sulfonamides highly active against dihydropteroate synthase form Toxoplasma gondii, Pneumocystis carinii, and Mycobacterium avium. Antimicrobial agents and chemotherapy 19960301
Properties