N-(2,4,6-trimethylpyridin-3-yl)benzenesulfonamide

Modify Date: 2026-07-23 11:47:50

N-(2,4,6-trimethylpyridin-3-yl)benzenesulfonamide Structure
N-(2,4,6-trimethylpyridin-3-yl)benzenesulfonamide structure
Common Name N-(2,4,6-trimethylpyridin-3-yl)benzenesulfonamide
CAS Number 34456-56-9 Molecular Weight 276.35400
Density 1.252g/cm3 Boiling Point 411.3ºC at 760mmHg
Molecular Formula C14H16N2O2S Melting Point N/A
MSDS N/A Flash Point 202.6ºC

 Names

Name 1-[(2R,4S,5R)-4-hydroxy-5-(tritiooxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.252g/cm3
Boiling Point 411.3ºC at 760mmHg
Molecular Formula C14H16N2O2S
Molecular Weight 276.35400
Flash Point 202.6ºC
Exact Mass 276.09300
PSA 67.44000
LogP 3.96140
InChIKey BLDIONVFHCVTJL-UHFFFAOYSA-N
SMILES Cc1cc(C)c(NS(=O)(=O)c2ccccc2)c(C)n1

 Bioassay

View more

Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
Name: High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
Source: Southern Research Institute
Target: HIV-1 Vif
External Id: HIV1-VIF_MS
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 Synonyms

3-Benzolsulfonamido-2,4,6-trimethylpyridin
3-Benzosulfamido-2,4,6-trimethylpyridin
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