138-42-1 | Benzenesulfonic acid, 4-nitro-

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$31.00	$22.00
1g	98%	in stock	$60.00	$42.00
5g	98%	in stock	$78.00	$54.00
25g	98%	in stock	$172.00	$120.00

Description

• Catalog Number: AA56577
• Chemical Name: Benzenesulfonic acid, 4-nitro-
• CAS Number: 138-42-1
• Molecular Formula: C6H5NO5S
• Molecular Weight: 203.1726
• MDL Number: MFCD09037353
• SMILES: O=N(=O)c1ccc(cc1)S(=O)(=O)O
• NSC Number: 5376

Computed Properties

• Complexity: 279
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.8

Literature

• 1-(4-Methyl-phen-yl)-3-phenyl-1H-pyrazol-5-yl 4-nitro-benzene-sulfonate.

  Acta crystallographica. Section E, Structure reports online 20120401

• 4-{2-[4-(Dimethyl-amino)-phen-yl]ethen-yl}-1-methyl-pyridinium 4-nitro-benzene-sulfonate.

  Acta crystallographica. Section E, Structure reports online 20120401

• 1H-1,2,4-Triazol-4-ium 4-nitro-benzene-sulfonate monohydrate.

  Acta crystallographica. Section E, Structure reports online 20111001

• Novel 2-substituted quinolin-4-yl-benzenesulfonate derivatives: synthesis, antiproliferative activity, and inhibition of cellular tubulin polymerization.

  ChemMedChem 20110606

• Activation of sulfonate ester based matrix metalloproteinase proinhibitors by hydrogen peroxide.

  Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry 20110201

• Triethyl-ammonium 4-nitro-benzene-sulfonate.

  Acta crystallographica. Section E, Structure reports online 20100701

• Copper powder-catalyzed regio- and stereoselective aminobromination of alpha,beta-unsaturated ketones with TsNH2 and NBS as nitrogen and halogen sources.

  The Journal of organic chemistry 20090206

• Highly stereoselective Saucy-Marbet rearrangement using chiral ynamides. Synthesis of highly substituted chiral homoallenyl alcohols.

  Organic letters 20030724

• The first stereoselective Ficini-Claisen rearrangement using chiral ynamides.

  Organic letters 20020418