Catalog No.:AA00EDTD

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

Name: Name:2-Methoxy-2-(1-naphthyl)propionic acid
Brand: AABLOCKS
SKU: AA00EDTD
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00EDTD

Chemical Name:

2-Methoxy-2-(1-naphthyl)propionic acid

CAS Number:

63628-25-1

Molecular Formula:

C14H14O3

Molecular Weight:

230.2592

MDL Number:

MFCD03093635

SMILES:

COC(c1cccc2c1cccc2)(C(=O)O)C

Properties

BP:

403.6°C at 760 mmHg

Form:

Solid

MP:

161-162°

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

289

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

Undefined Atom Stereocenter Count:

XLogP3:

2.9

Upstream Synthesis Route

90-11-9

63628-25-1

[1]TetrahedronLetters,2014,vol.55,#30,p.4114-4116

247130-25-2

63628-25-1

[1]TetrahedronLetters,2014,vol.55,#30,p.4114-4116

Downstream Synthesis Route

2216-51-5

63628-25-1

220167-99-7

220168-00-3

[1]TetrahedronAsymmetry,2000,vol.11,p.1249-1253

63628-25-1

(4Z,17Z,27E)-(R)-29-Hydroxy-hentriaconta-4,17,27-triene-2,20,30-triynoicacidmethylester

(4Z,17Z,27E)-(R)-29-(2-Methoxy-2-naphthalen-1-yl-propionyloxy)-hentriaconta-4,17,27-triene-2,20,30-triynoicacidmethylester

[1]JournalofNaturalProducts,2002,vol.65,p.1353-1356

63628-25-1

102691-93-0

[1]TetrahedronAsymmetry,2000,vol.11,p.1249-1253

63628-25-1

63628-26-2

[1]TetrahedronAsymmetry,2000,vol.11,p.1249-1253

Literature

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

Journal: Bioscience, biotechnology, and biochemistry 20080901

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

Journal: Journal of chromatography. A 20060602

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

Journal: Chirality 20060201

Title: 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.

Journal: Chirality 20051101

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

Journal: Chirality 20050505

Title: 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.

Journal: Chirality 20050101

Title: 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.

Journal: Chirality 20041101

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

Journal: Chirality 20040101

Title: 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.

Journal: Chirality 20020101

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

Journal: Enantiomer 20020101

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