1137-41-3 | 4-Aminobenzophenone

Packsize	Purity	Availability	Price	Discounted Price
10g	95%	in stock	$12.00	$9.00
25g	95%	in stock	$18.00	$13.00
100g	95%	in stock	$62.00	$44.00
500g	98%	in stock	$289.00	$203.00

Description

• Catalog Number: AA11940
• Chemical Name: 4-Aminobenzophenone
• CAS Number: 1137-41-3
• Molecular Formula: C13H11NO
• Molecular Weight: 197.2325
• MDL Number: MFCD00007895
• SMILES: Nc1ccc(cc1)C(=O)c1ccccc1
• NSC Number: 7665

Computed Properties

• Complexity: 213
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 2.7

Literature

• Biodegradation of malachite green by Pseudomonas sp. strain DY1 under aerobic condition: characteristics, degradation products, enzyme analysis and phytotoxicity.

  Ecotoxicology (London, England) 20110301

• Biophysical investigation of the mode of inhibition of tetramic acids, the allosteric inhibitors of undecaprenyl pyrophosphate synthase.

  Biochemistry 20100629

• Flexible two-dimensional square-grid coordination polymers: structures and functions.

  International journal of molecular sciences 20100101

• Nickel-NHC-catalyzed alpha-arylation of acyclic ketones and amination of haloarenes and unexpected preferential N-arylation of 4-aminopropiophenone.

  The Journal of organic chemistry 20070706

• Stimuli-responsive properties of N-isopropylacrylamide-based ultrathin hydrogel films prepared by photo-cross-linking.

  Langmuir : the ACS journal of surfaces and colloids 20060620

• Non-peptidic small-molecule inhibitors of the single-chain hepatitis C virus NS3 protease/NS4A cofactor complex discovered by structure-based NMR screening.

  Journal of medicinal chemistry 20040506

• Inversion of 4-methoxybenzophenone triplet in aqueous solutions.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20020901

• Non-thiol farnesyltransferase inhibitors: evaluation of different AA(X)-peptidomimetic substructures in combination with arylic cysteine replacements.

  Archiv der Pharmazie 20020401