CAS 708-06-5

2-Hidroxi-1-naftaldeído

Descrição:

2-Hidroxi-1-naftaldeído, com o número CAS 708-06-5, é um composto orgânico que pertence à classe dos derivados do naftaleno. Apresenta um grupo hidroxila (-OH) e um grupo aldeído (-CHO) ligados a um anel de naftaleno, especificamente nas posições 1 e 2, respectivamente. Este composto é tipicamente um sólido à temperatura ambiente e é conhecido por suas propriedades aromáticas, que contribuem para suas potenciais aplicações na síntese orgânica e como bloco de construção no desenvolvimento de vários compostos químicos. Exibe boa solubilidade em solventes orgânicos como etanol e éter, enquanto é menos solúvel em água devido à sua estrutura hidrofóbica de naftaleno. 2-Hidroxi-1-naftaldeído pode participar de várias reações químicas, incluindo condensação e oxidação, tornando-o útil na síntese de corantes, produtos farmacêuticos e outros materiais orgânicos. Além disso, seu grupo hidroxila pode se envolver em ligações de hidrogênio, influenciando sua reatividade e interações em diferentes ambientes 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

Chave 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)

Cor e Forma: 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%

Cor e Forma: 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%

Cor e Forma: brown solid

Peso molecular: 172.18g/mol

Ref: 54-OR8817

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

Fórmula: C₁₁H₈O₂

Pureza: ≥ 90.0%

Cor e Forma: 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%

Cor e Forma: Solid

Peso molecular: 172.183

Ref: 10-F358223

1-Formylnaphthalen-2-ol

Produto Controlado

CAS: 708-06-5

Fórmula: C₁₁H₈O₂

Cor e Forma: 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%

Cor e Forma: Solid

Peso molecular: 172.18 g/mol

Ref: 3D-FH02093