CAS 708-06-5

2-Idrossi-1-naftaldeide

Descrizione:

2-Idrossi-1-naftaldeide, con il numero CAS 708-06-5, è un composto organico che appartiene alla classe dei derivati del naftalene. Presenta un gruppo idrossile (-OH) e un gruppo aldeidico (-CHO) attaccati a un anello di naftalene, specificamente nelle posizioni 1 e 2, rispettivamente. Questo composto è tipicamente un solido a temperatura ambiente ed è noto per le sue proprietà aromatiche, che contribuiscono alle sue potenziali applicazioni nella sintesi organica e come blocco di costruzione nello sviluppo di vari composti chimici. Mostra una buona solubilità in solventi organici come etanolo ed etere, mentre è meno solubile in acqua a causa della sua struttura idrofobica di naftalene. 2-Idrossi-1-naftaldeide può partecipare a varie reazioni chimiche, inclusa la condensazione e l'ossidazione, rendendolo utile nella sintesi di coloranti, prodotti farmaceutici e altri materiali organici. Inoltre, il suo gruppo idrossile può impegnarsi in legami idrogeno, influenzando la sua reattività e interazioni in diversi ambienti chimici.

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

Sinonimi:

• 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

Purezza: >98.0%(GC)(T)

Colore e forma: Light orange to Yellow to Green powder to crystal

Peso molecolare: 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

Purezza: 98%

Colore e forma: White to yellow to pale brown, Powder

Peso molecolare: 172.18

Ref: 02-B23951

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

2-Hydroxy-1-naphthaldehyde

Formula: C₁₁H₈O₂

Purezza: 98%

Colore e forma: brown solid

Peso molecolare: 172.18g/mol

Ref: 54-OR8817

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

Formula: C₁₁H₈O₂

Purezza: ≥ 90.0%

Colore e forma: Light-yellow to green or brown powder

Peso molecolare: 172.18

Ref: 7W-GK6521

2-hydroxynaphthalene-1-carbaldehyde

CAS: 708-06-5

Formula: C₁₁H₈O₂

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 172.183

Ref: 10-F358223

1-Formylnaphthalen-2-ol

Prodotto controllato

CAS: 708-06-5

Formula: C₁₁H₈O₂

Colore e forma: Neat

Peso molecolare: 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

Purezza: Min. 95%

Colore e forma: Solid

Peso molecolare: 172.18 g/mol

Ref: 3D-FH02093