724696
3-Aminobenzenesulfonamide
98%
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About This Item
Empirical Formula (Hill Notation):
C6H8N2O2S
CAS Number:
Molecular Weight:
172.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
form
solid
mp
141-143 °C
SMILES string
Nc1cccc(c1)S(N)(=O)=O
InChI
1S/C6H8N2O2S/c7-5-2-1-3-6(4-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)
InChI key
JPVKCHIPRSQDKL-UHFFFAOYSA-N
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Annabel Meyer et al.
PloS one, 8(9), e73536-e73536 (2013-09-17)
Understanding factors driving the ecology of N cycling microbial communities is of central importance for sustainable land use. In this study we report changes of abundance of denitrifiers, nitrifiers and nitrogen-fixing microorganisms (based on qPCR data for selected functional genes)
Tanzeela Abdul Fattah et al.
Bioorganic chemistry, 82, 123-128 (2018-10-13)
We describe the synthesis of a series of novel 1-aroyl/acyl-3-(3-aminosulfonylphenyl) thioureas (4a-k) acting as human carbonic anhydrase (hCA, EC 4.2.1.1) inhibitors. Reaction of alkyl/aryl isothiocyanates with 3-aminobenzenesulfonamide afforded a series of the title compounds incorporating a variety of short as
Suleyman Akocak et al.
Bioorganic chemistry, 103, 104204-104204 (2020-09-06)
Building on the conclusions of previous inhibition studies with pyridinium-benzenesulfonamides from our team and on the X-ray crystal structure of the lead compound identified, a series of 24 pyridinium derivatives of 3-aminobenzenesulfonamide was synthesized and investigated for carbonic anhydrase inhibition.
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