120-23-0 | 2-Naphthoxyacetic acid

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$8.00	$6.00
100g	98%	in stock	$24.00	$17.00
500g	98%	in stock	$96.00	$68.00
5kg	≥ 98% (Assay)	in stock	$936.00	$656.00
10kg	≥ 98% (Assay)	in stock	$1,760.00	$1,232.00

Description

• Catalog Number: AA33498
• Chemical Name: 2-Naphthoxyacetic acid
• CAS Number: 120-23-0
• Molecular Formula: C12H10O3
• Molecular Weight: 202.2060
• MDL Number: MFCD00004066
• SMILES: OC(=O)COc1ccc2c(c1)cccc2
• NSC Number: 2070

Computed Properties

• Complexity: 227
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 2.5

Upstream Synthesis Route

2-Naphthoxyacetic acid, also known as 2-NOAA, is a versatile compound commonly employed in chemical synthesis for various applications. Its primary use lies in the field of organic chemistry, where it serves as a key intermediate in the synthesis of numerous pharmaceuticals, agrochemicals, and other fine chemicals.In chemical synthesis, 2-Naphthoxyacetic acid plays a crucial role as a precursor in the production of a wide range of organic compounds. One of its notable applications is in the synthesis of plant growth regulators, where it acts as a vital component for the creation of growth-promoting substances. Additionally, 2-NOAA is utilized in the preparation of herbicides and insecticides, contributing to the development of effective pest control agents.Furthermore, this compound is valued for its ability to participate in various reactions, such as esterification, hydrolysis, and condensation, making it an essential building block in the creation of complex organic molecules. Its high reactivity and compatibility with other reagents make it a valuable tool in the hands of synthetic chemists, enabling the efficient production of diverse chemical compounds.Overall, 2-Naphthoxyacetic acid's significance in chemical synthesis extends across multiple industries, highlighting its importance as a versatile and indispensable component in the creation of a wide array of valuable products.

Literature

• Application of photoremovable protecting group for controlled release of plant growth regulators by sunlight.

  Journal of photochemistry and photobiology. B, Biology 20120604

• Simultaneous determination of plant growth regulators 1-naphthylacetic acid and 2-naphthoxyacetic acid in fruit and vegetable samples by room temperature phosphorescence.

  Phytochemical analysis : PCA 20120101

• Effects of two plant growth regulators, indole-3-acetic acid and β-naphthoxyacetic acid, on genotoxicity in Drosophila SMART assay and on proliferation and viability of HEK293 cells from the perspective of carcinogenesis.

  Toxicology and industrial health 20111001

• Simultaneous determination of 13 phytohormones in oilseed rape tissues by liquid chromatography-electrospray tandem mass spectrometry and the evaluation of the matrix effect.

  Journal of separation science 20110301

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

  Sensors (Basel, Switzerland) 20110101

• Non-invasive quantification of endogenous root auxin transport using an integrated flux microsensor technique.

  The Plant journal : for cell and molecular biology 20100901

• Auxin influx inhibitors 1-NOA, 2-NOA, and CHPAA interfere with membrane dynamics in tobacco cells.

  Journal of experimental botany 20100801

• Fluorescence-based comparative binding studies of the supramolecular host properties of PAMAM dendrimers using anilinonaphthalene sulfonates: unusual host-dependent fluorescence titration behavior.

  Sensors (Basel, Switzerland) 20100101

• Determination of naphthalene by competitive fluorescence immunoassay.

  Environmental monitoring and assessment 20090701

• Bis[μ-2-(2-naphth-oxy)acetato]bis-{aqua[2-(2-naphth-oxy)acetato]zinc(II)}.

  Acta crystallographica. Section E, Structure reports online 20090501

• Identification of auxins by a chemical genomics approach.

  Journal of experimental botany 20080701

• Determination of plant hormones in fertilizers by high-performance liquid chromatography with photodiode array detection: method development and single-laboratory validation.

  Journal of AOAC International 20080101

• Determination of ibuprofen and flurbiprofen in pharmaceuticals by capillary zone electrophoresis.

  Journal of pharmaceutical and biomedical analysis 20060616

• Proliferation potential of 18-month-old callus of Ananas comosus L. cv. Moris.

  TheScientificWorldJournal 20060101

• Specificity patterns indicate that auxin exporters and receptors are the same proteins.

  Plant biology (Stuttgart, Germany) 20050101

• 2-Amino-2-thiazoline and its 1:1 organic salt with 2-naphthoxyacetic acid.

  Acta crystallographica. Section C, Crystal structure communications 20040901

• 2-(2-Naphthyloxy)acetate derivatives. I. A new class of antiamnesic agents.

  Acta crystallographica. Section C, Crystal structure communications 20030801

• 2-(2-Naphthyloxy)acetate derivatives. II. A new class of antiamnesic agents.

  Acta crystallographica. Section C, Crystal structure communications 20030801

• Intercalibration of chromatographic methods for auxino phytodrugs in Solanaceae.

  Journal of chromatography. A 20030418

• (2-Naphthoxy)acetyl chloride, a simple fluorescent reagent.

  Journal of chromatography. A 20030214

• Species differences in ligand specificity of auxin-controlled elongation and auxin transport: comparing Zea and Vigna.

  Planta 20021201

• Structure of the complex of beta-cyclodextrin with beta-naphthyloxyacetic acid in the solid state and in aqueous solution.

  Carbohydrate research 20010508