CAS 708-06-5

2-Hidroxi-1-naftaldehído

Descripción:

2-Hidroxi-1-naftaldehído, con el número CAS 708-06-5, es un compuesto orgánico que pertenece a la clase de los derivados del naftaleno. Presenta un grupo hidroxilo (-OH) y un grupo aldehído (-CHO) unidos a un anillo de naftaleno, específicamente en las posiciones 1 y 2, respectivamente. Este compuesto es típicamente un sólido a temperatura ambiente y es conocido por sus propiedades aromáticas, que contribuyen a sus posibles aplicaciones en la síntesis orgánica y como bloque de construcción en el desarrollo de varios compuestos químicos. Exhibe buena solubilidad en disolventes orgánicos como el etanol y el éter, mientras que es menos soluble en agua debido a su estructura hidrofóbica de naftaleno. 2-Hidroxi-1-naftaldehído puede participar en varias reacciones químicas, incluyendo condensación y oxidación, lo que lo hace útil en la síntesis de colorantes, productos farmacéuticos y otros materiales orgánicos. Además, su grupo hidroxilo puede participar en enlaces de hidrógeno, influyendo en su reactividad e interacciones en diferentes entornos químicos.

Fórmula: C₁₁H₈O₂

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

Clave InChI: InChIKey=NTCCNERMXRIPTR-UHFFFAOYSA-N

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

Sinónimos:

• 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

Fórmula: C₁₁H₈O₂

Pureza: >98.0%(GC)(T)

Forma y color: Light orange to Yellow to Green powder to crystal

Peso molecular: 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

Fórmula: C₁₁H₈O₂

Pureza: 98%

Forma y color: White to yellow to pale brown, Powder

Peso molecular: 172.18

Ref: 02-B23951

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

2-Hydroxy-1-naphthaldehyde

Fórmula: C₁₁H₈O₂

Pureza: 98%

Forma y color: brown solid

Peso molecular: 172.18g/mol

Ref: 54-OR8817

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

Fórmula: C₁₁H₈O₂

Pureza: ≥ 90.0%

Forma y color: Light-yellow to green or brown powder

Peso molecular: 172.18

Ref: 7W-GK6521

2-hydroxynaphthalene-1-carbaldehyde

CAS: 708-06-5

Fórmula: C₁₁H₈O₂

Pureza: 98%

Forma y color: Solid

Peso molecular: 172.183

Ref: 10-F358223

1-Formylnaphthalen-2-ol

Producto controlado

CAS: 708-06-5

Fórmula: C₁₁H₈O₂

Forma y color: Neat

Peso molecular: 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

Fórmula: C₁₁H₈O₂

Pureza: Min. 95%

Forma y color: Solid

Peso molecular: 172.18 g/mol

Ref: 3D-FH02093