63628-25-1 | 2-Methoxy-2-(1-naphthyl)propionic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$97.00	$68.00
5g	98%	in stock	$297.00	$208.00
10g	98%	in stock	$463.00	$324.00
25g	98%	in stock	$968.00	$678.00

Description

• Catalog Number: AG70989
• Chemical Name: 2-Methoxy-2-(1-naphthyl)propionic acid
• CAS Number: 63628-25-1
• Molecular Formula: C14H14O3
• Molecular Weight: 230.25915999999998
• MDL Number: MFCD03093635
• SMILES: COC(c1cccc2c1cccc2)(C(=O)O)C

Computed Properties

• Complexity: 289
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 2.9

Literature

• Preparation of single-enantiomer biofunctional molecules with (S)-2-methoxy-2-(1-naphthyl)propanoic acid.

  Bioscience, biotechnology, and biochemistry 20080901

• Preparation of single-enantiomer 2-methyl-4-heptanol, a pheromone of Metamasius hemipterus, using (S)-2-methoxy-2-(1-naphthyl)propionic acid.

  Journal of chromatography. A 20060602

• Preparation of enantiopure Wieland-Miescher ketone and derivatives by the MalphaNP acid method: substituent effect on the HPLC separation.

  Chirality 20060201

• Investigations of molecular recognition aspects related to the enantiomer separation of 2-methoxy-2-(1-naphthyl)propionic acid using quinine carbamate as chiral selector: An NMR and FT-IR spectroscopic as well as X-ray crystallographic study.

  Chirality 20051101

• Synthesis of enantiopure phthalides including 3-butylphthalide, a fragrance component of celery oil, and determination of their absolute configurations.

  Chirality 20050505

• Enantiomer separation of a powerful chiral auxiliary, 2-methoxy-2-(1-naphthyl)propionic acid by liquid chromatography using chiral anion exchanger-type stationary phases in polar-organic mode; investigation of molecular recognition aspects.

  Chirality 20050101

• MalphaNP acid, a powerful chiral molecular tool for preparation of enantiopure alcohols by resolution and determination of their absolute configurations by the (1)H NMR anisotropy method.

  Chirality 20041101

• Absolute configuration of the thyroid hormone analog KAT-2003 as determined by the 1H NMR anisotropy method with a novel chiral auxiliary, MalphaNP acid.

  Chirality 20040101

• Practical enantioresolution of alcohols with 2-methoxy-2-(1-naphthyl)propionic acid and determination of their absolute configurations by the (1)H NMR anisotropy method.

  Chirality 20020101

• Crystalline state conformation of 2-methoxy-2-(1-naphthyl)propionic acid ester.

  Enantiomer 20020101