118-31-0 | 1-Naphthalenemethylamine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$11.00	$8.00
5g	98%	in stock	$29.00	$21.00
10g	98%	in stock	$53.00	$38.00
25g	98%	in stock	$121.00	$85.00

Description

• Catalog Number: AB43420
• Chemical Name: 1-Naphthalenemethylamine
• CAS Number: 118-31-0
• Molecular Formula: C11H11N
• Molecular Weight: 157.2117
• MDL Number: MFCD00004048
• SMILES: NCc1cccc2c1cccc2

Computed Properties

• Complexity: 144
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.1

Literature

• Synthesis of a novel polyurethane-based-magnetic imprinted polymer for the selective optical detection of 1-naphthylamine in drinking water.

  Biosensors & bioelectronics 20110715

• Luminescence sensors applied to water analysis of organic pollutants--an update.

  Sensors (Basel, Switzerland) 20110101

• (1-Naphthyl-meth-yl)ammonium chloride.

  Acta crystallographica. Section E, Structure reports online 20100301

• HPLC method validation studies on a specific assay for monomethoxypoly(ethylene glycol) succinimido carbonate (mPEG-SC).

  Journal of pharmaceutical and biomedical analysis 20090908

• Chemometric-assisted MIP-optosensing system for the simultaneous determination of monoamine naphthalenes in drinking waters.

  Talanta 20090415

• Conformation-selective synthesis and binding properties of N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide.

  The Journal of organic chemistry 20080718

• Chiral amplification in macromolecular helicity assisted by noncovalent interaction with achiral amines and memory of the helical chirality.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20041004

• Exploring the binding mode of semicarbazide-sensitive amine oxidase/VAP-1: identification of novel substrates with insulin-like activity.

  Journal of medicinal chemistry 20040923

• A novel organic intercalation system with layered polymer crystals as the host compounds derived from 1,3-diene carboxylic acids.

  Journal of the American Chemical Society 20021120