2210-24-4 | N-Phenylacrylamide

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$7.00	$5.00
1g	97%	in stock	$11.00	$8.00
5g	97%	in stock	$20.00	$14.00
25g	97%	in stock	$88.00	$62.00
100g	97%	in stock	$287.00	$201.00

Description

• Catalog Number: AF62017
• Chemical Name: N-Phenylacrylamide
• CAS Number: 2210-24-4
• Molecular Formula: C9H9NO
• Molecular Weight: 147.1739
• MDL Number: MFCD00080617
• SMILES: C=CC(=O)Nc1ccccc1
• NSC Number: 6857

Computed Properties

• Complexity: 148
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 1.8

Literature

• Synthesis, biological evaluation and molecular docking studies of 3-(1,3-diphenyl-1H-pyrazol-4-yl)-N-phenylacrylamide derivatives as inhibitors of HDAC activity.

  Bioorganic & medicinal chemistry 20120715

• Discovery and structure-activity relationship of potent and selective covalent inhibitors of transglutaminase 2 for Huntington's disease.

  Journal of medicinal chemistry 20120209

• A comparative assessment of α-lipoic acid N-phenylamides as non-steroidal androgen receptor antagonists both on and off gold nanoparticles.

  Bioorganic chemistry 20120201

• Competing pathways control host resistance to virus via tRNA modification and programmed ribosomal frameshifting.

  Molecular systems biology 20120101

• Effects of dynamical couplings in IR spectra of the hydrogen bond in N-phenylacrylamide crystals.

  The journal of physical chemistry. A 20110505

• Analysis of wheat extracts for ochratoxin A by molecularly imprinted solid-phase extraction and pulsed elution.

  Analytical and bioanalytical chemistry 20040401

• Tris(2-carboxyethyl)phosphine stabilization of RNA: comparison with dithiothreitol for use with nucleic acid and thiophosphoryl chemistry.

  Analytical biochemistry 20040201

• Enantioselective [6pi]-photocyclization reaction of an acrylanilide mediated by a chiral host. Interplay between enantioselective ring closure and enantioselective protonation.

  The Journal of organic chemistry 20030207