CAS 6953-22-6

5-(Fenilmetoxi)-1H-indol-3-carboxaldeído

Descrição:

5-(Fenilmetoxi)-1H-indol-3-carboxaldeído, com o número CAS 6953-22-6, é um composto orgânico caracterizado por sua estrutura de indol, que é um composto bicíclico consistindo em um anel de benzeno fundido a um anel de pirrol. Este composto apresenta um grupo fenilmetóxi, que melhora sua solubilidade e reatividade. A presença do grupo funcional aldeído na posição 3 do anel de indol torna-o um intermediário versátil na síntese orgânica, particularmente no desenvolvimento de produtos farmacêuticos e agroquímicos. Exibe propriedades típicas dos derivados de indol, como atividade biológica potencial, incluindo efeitos antimicrobianos e anticancerígenos. O composto provavelmente será um sólido à temperatura ambiente e pode ser sensível à luz e à umidade, exigindo manuseio e armazenamento cuidadosos. Sua reatividade pode ser atribuída à natureza eletrofílica do grupo aldeído, permitindo várias transformações químicas. No geral, 5-(Fenilmetoxi)-1H-indol-3-carboxaldeído é um composto significativo na química medicinal e na química orgânica sintética.

Fórmula: C₁₆H₁₃NO₂

InChI: InChI=1S/C16H13NO2/c18-10-13-9-17-16-7-6-14(8-15(13)16)19-11-12-4-2-1-3-5-12/h1-10,17H,11H2

Chave InChI: InChIKey=DJGNUBADRQIDNQ-UHFFFAOYSA-N

SMILES: C(=O)C=1C=2C(NC1)=CC=C(OCC3=CC=CC=C3)C2

Sinónimos:

• 1H-Indole-3-carboxaldehyde, 5-(phenylmethoxy)-
• 5-(Phenylmethoxy)-1H-Indole-3-Carbaldehyde
• 5-(Phenylmethoxy)-1H-indole-3-carboxaldehyde
• 5-Benzyloxy-1H-indole-3-carboxaldehyde
• 5-Benzyloxy-3-formylindole
• 5-Benzyloxy-3-indolecarboxaldehyde
• Indole-3-carboxaldehyde, 5-(benzyloxy)-
• NSC 71049
• 5-BENZYLOXYINDOLE-3-CARBOXALDEHYDE
• 5-Benzyloxy-3-formyl-1H-indole
• 5-Benzyloxy-3-formaldehyde
• 5-(BENZYLOXY)-1H-INDOLE-3-CARBALDEHYDE
• 5-BENZYLOXY INDOLE-3-CARBOXYALDEHYDE
• 5-BENZYLOXYINDOLE-3-ALDEHYDE
• 5-BENZYLOXYINDOLE-3-CARBALDEHYDE
• 5-Benzyloxyindole-3-carboxaldehyde ,98%
• 5-BENZYLOXYINDOLE-3-FORMALDEHYDE

5-Benzyloxyindole-3-carboxaldehyde, 98%

CAS: 6953-22-6

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Fórmula: C₁₆H₁₃NO₂

Pureza: 98%

Cor e Forma: Pale yellow to Dark Yellow or Pale Cream to Brown, Powder

Peso molecular: 251.29

Ref: 02-L01117

5-Benzyloxyindole-3-carboxaldehyde

CAS: 6953-22-6

Pureza: 98.0%

Cor e Forma: Solid, Crystalline Powder or Powder

Peso molecular: 251.28500366210938

Ref: 10-F012742

5-Benzyloxy-3-formylindole

CAS: 6953-22-6

Fórmula: C₁₆H₁₃NO₂

Pureza: 97%

Cor e Forma: Solid

Peso molecular: 251.2799

Ref: IN-DA00IBY8

5-Benzyloxyindole-3-carboxaldehyde

CAS: 6953-22-6

Fórmula: C₁₆H₁₃NO₂

Peso molecular: 251.28

Ref: 7W-GK5386

5-(Benzyloxy)-1H-indole-3-carboxaldehyde

CAS: 6953-22-6

5-(Benzyloxy)-1H-indole-3-carboxaldehyde

Fórmula: C₁₆H₁₃NO₂

Pureza: ≥95%

Cor e Forma: Powder

Peso molecular: 251.28g/mol

Ref: 54-OR1344

5-Benzyloxyindole-3-carboxaldehyde

CAS: 6953-22-6

5-Benzyloxyindole-3-carboxaldehyde is a high purity chemical that is used as a reagent in organic synthesis.

Fórmula: C₁₆H₁₃NO₂

Pureza: Min. 98.0 Area-%

Peso molecular: 251.29 g/mol

Ref: 3D-B-1870

5-Benzyloxyindole-3-carboxaldehyde

CAS: 6953-22-6

5-Benzyloxyindole-3-carboxaldehyde is a merocyanine dye that can be used as an antimycobacterial agent in cell culture. It is also fluorescent and has been shown to inhibit the growth of Mycobacterium tuberculosis. 5-Benzyloxyindole-3-carboxaldehyde has been synthesised by reacting 5,5′-dibenzoyloxydihydropyrene with indole and benzaldehyde. The hydrolysis of this compound yields the corresponding carboxylic acid and benzoic acid, which are then converted to the desired product by action of sodium ethoxide. Merocyanine dyes are characterized by a distinctive absorption band in the visible region at about 540 nm. These compounds have also been shown to inhibit renal cells, which may be due to their ability to act as nucleophiles or tautomers.

Fórmula: C₁₆H₁₃NO₂

Pureza: Min. 95%

Cor e Forma: Off-White Powder

Peso molecular: 251.28 g/mol

Ref: 3D-FB18516