21969-70-0 | 2-Anilinoacetamide

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$131.00	$92.00
1g	98%	in stock	$325.00	$228.00
5g	98%	in stock	$946.00	$662.00
10g	98%	in stock	$1,412.00	$989.00
25g	98%	in stock	$2,966.00	$2,077.00

Description

• Catalog Number: AF63224
• Chemical Name: 2-Anilinoacetamide
• CAS Number: 21969-70-0
• Molecular Formula: C8H10N2O
• Molecular Weight: 150.1778
• MDL Number: MFCD08691108
• SMILES: NC(=O)CNc1ccccc1

Computed Properties

• Complexity: 130
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Literature

• Synthesis of optically active amino acid derivatives via dynamic kinetic resolution.

  The Journal of organic chemistry 20091218

• N-(Anilinoethyl)amides: design and synthesis of metabolically stable, selective melatonin receptor ligands.

  ChemMedChem 20091001

• Investigation of the terminal P4 domain in a series of D-phenylglycinamide-based factor Xa inhibitors.

  Bioorganic & medicinal chemistry letters 20071215

• Solid state NMR analysis of the dipolar couplings within and between distant CF3-groups in a membrane-bound peptide.

  Journal of magnetic resonance (San Diego, Calif. : 1997) 20061101

• Novel phenylamino acetamide derivatives as potent and selective kappa opioid receptor agonists.

  Bioorganic & medicinal chemistry letters 20060201

• Design of selective phenylglycine amide tissue factor/factor VIIa inhibitors.

  Bioorganic & medicinal chemistry letters 20050201

• A four component coupling strategy for the synthesis of D-phenylglycinamide-derived non-covalent factor Xa inhibitors.

  Bioorganic & medicinal chemistry letters 20030721

• Enzyme distribution derived from macroscopic particle behavior of an industrial immobilized penicillin-G acylase.

  Biotechnology progress 20030101

• A two-step, one-pot enzymatic synthesis of cephalexin from D-phenylglycine nitrile.

  Biotechnology and bioengineering 20020805

• Penicillin acylase-catalyzed ampicillin synthesis using a pH gradient: a new approach to optimization.

  Biotechnology and bioengineering 20020605