CAS 708-06-5

2-Hydroxy-1-naphthaldehyde

Description:

2-Hydroxy-1-naphthaldehyde, with the CAS number 708-06-5, is an organic compound that belongs to the class of naphthalene derivatives. It features a hydroxyl group (-OH) and an aldehyde group (-CHO) attached to a naphthalene ring, specifically at the 1 and 2 positions, respectively. This compound is typically a solid at room temperature and is known for its aromatic properties, which contribute to its potential applications in organic synthesis and as a building block in the development of various chemical compounds. It exhibits good solubility in organic solvents such as ethanol and ether, while being less soluble in water due to its hydrophobic naphthalene structure. 2-Hydroxy-1-naphthaldehyde can participate in various chemical reactions, including condensation and oxidation, making it useful in the synthesis of dyes, pharmaceuticals, and other organic materials. Additionally, its hydroxyl group can engage in hydrogen bonding, influencing its reactivity and interactions in different chemical environments.

Formula: C₁₁H₈O₂

InChI: InChI=1/C11H8O2/c12-7-10-9-4-2-1-3-8(9)5-6-11(10)13/h1-7,13H

InChI key: InChIKey=NTCCNERMXRIPTR-UHFFFAOYSA-N

SMILES: C(=O)C=1C2=C(C=CC1O)C=CC=C2

Synonyms:

• 1-Formyl-2-Hydroxynaphthalene
• 1-Formyl-2-naphthol
• 1-Formylnaphthalen-2-ol
• 1-Naphthaldehyde, 2-hydroxy-
• 1-Naphthalenecarboxaldehyde, 2-hydroxy-
• 2-Hidroxi-1-Naftaldehido
• 2-Hydroxy-1-formylnaphthalene
• 2-Hydroxy-1-naphtaldehyde
• 2-Hydroxy-1-naphthaldehyd
• 2-Hydroxy-1-naphthalenealdehyde
• 2-Hydroxy-1-naphthalenecarboxaldehyde
• 2-Hydroxy-α-naphthaldehyde
• 2-Hydroxynaphthaldehyde
• 2-Hydroxynaphthalenecarboxaldehyde
• 2-Hydroxynaphthyl-1-carboxaldehyde
• 2-Hyroxy-1-Naphthyldhyd
• 2-Naphthol-1-aldehyde
• Naphthaldehyde, 2-Hydroxy-
• Nc 014
• Nsc 2104
• Nsc 402586
• Timtec-Bb Sbb003835
• β-Hydroxy-α-naphthaldehyde
• β-Hydroxynaphthaldehyde
• 1-Formyl-2-hydroxy-naphthalene
• AKOS 90775
• AKOS BBS-00003198
• LABOTEST-BB LT00942158
• 2-hydroxy-1-naphthalenecarboxaldehyd
• 2-HYDROXY-NAPHTHALDEHYDE
• 2-Hydroxy-1-naphthylaldehyde
• 2-Hydroxy-alpha-naphthaldehyde
• 2-Hydroxy-1-napthaldehyde
• 1-Hydroxy-2-naphthalenecarboxaldehyde
• 2-Hydroxy-1-naphthalaldehyde

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

Formula: C₁₁H₈O₂

Purity: >98.0%(GC)(T)

Color and Shape: Light orange to Yellow to Green powder to crystal

Molecular weight: 172.18

Ref: 3B-H0275

2-Hydroxy-1-naphthaldehyde, 98%

CAS: 708-06-5

2-Hydroxy-1-naphthaldehyde is used in Merrified-type synthesis to deterime free amino acid groups in polymers. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original

Formula: C₁₁H₈O₂

Purity: 98%

Color and Shape: White to yellow to pale brown, Powder

Molecular weight: 172.18

Ref: 02-B23951

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

2-Hydroxy-1-naphthaldehyde

Formula: C₁₁H₈O₂

Purity: 98%

Color and Shape: brown solid

Molecular weight: 172.18g/mol

Ref: 54-OR8817

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

Formula: C₁₁H₈O₂

Purity: ≥ 90.0%

Color and Shape: Light-yellow to green or brown powder

Molecular weight: 172.18

Ref: 7W-GK6521

2-hydroxynaphthalene-1-carbaldehyde

CAS: 708-06-5

Formula: C₁₁H₈O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 172.183

Ref: 10-F358223

1-Formylnaphthalen-2-ol

Controlled Product

CAS: 708-06-5

Formula: C₁₁H₈O₂

Color and Shape: Neat

Molecular weight: 172.18

Ref: TR-F700825

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

2-Hydroxy-1-naphthaldehyde is a redox potential chemical that has been shown to have anticancer activity in vitro and in vivo. It inhibits the growth of cells by binding to iron, which is important for many biological processes including DNA synthesis. 2-Hydroxy-1-naphthaldehyde has also been shown to have metal carbonyl reactivity and fluorescence properties that may be useful as a fluorescent probe. 2-Hydroxy-1-naphthaldehyde binds to iron ions through hydrogen bonding interactions, forming an octahedral complex with six ligands. The compound also has coordination geometry that can be described as either trigonal bipyramidal or square planar, depending on the solvent used. This data was obtained by x-ray diffraction studies of crystalline solids. The compound's Langmuir adsorption isotherm was found to be linear at low concentrations and shifted to nonlinear behavior at higher concentrations. The

Formula: C₁₁H₈O₂

Purity: Min. 95%

Color and Shape: Solid

Molecular weight: 172.18 g/mol

Ref: 3D-FH02093