CAS 6953-22-6

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

Description:

5-(Phenylmethoxy)-1H-indole-3-carboxaldehyde, with the CAS number 6953-22-6, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a phenylmethoxy group, which enhances its solubility and reactivity. The presence of the aldehyde functional group at the 3-position of the indole ring makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It exhibits properties typical of indole derivatives, such as potential biological activity, including antimicrobial and anticancer effects. The compound is likely to be a solid at room temperature and may be sensitive to light and moisture, necessitating careful handling and storage. Its reactivity can be attributed to the electrophilic nature of the aldehyde group, allowing for various chemical transformations. Overall, 5-(Phenylmethoxy)-1H-indole-3-carboxaldehyde is a significant compound in medicinal chemistry and synthetic organic chemistry.

Formula: 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

InChI key: InChIKey=DJGNUBADRQIDNQ-UHFFFAOYSA-N

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

Synonyms:

• 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

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 Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₁₆H₁₃NO₂

Purity: 98%

Color and Shape: Pale yellow to Dark Yellow or Pale Cream to Brown, Powder

Molecular weight: 251.29

Ref: 02-L01117

5-Benzyloxyindole-3-carboxaldehyde

CAS: 6953-22-6

Purity: 98.0%

Color and Shape: Solid, Crystalline Powder or Powder

Molecular weight: 251.28500366210938

Ref: 10-F012742

5-Benzyloxy-3-formylindole

CAS: 6953-22-6

Formula: C₁₆H₁₃NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 251.2799

Ref: IN-DA00IBY8

5-Benzyloxyindole-3-carboxaldehyde

CAS: 6953-22-6

Formula: C₁₆H₁₃NO₂

Molecular weight: 251.28

Ref: 7W-GK5386

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

CAS: 6953-22-6

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

Formula: C₁₆H₁₃NO₂

Purity: ≥95%

Color and Shape: Powder

Molecular weight: 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.

Formula: C₁₆H₁₃NO₂

Purity: Min. 98.0 Area-%

Molecular weight: 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.

Formula: C₁₆H₁₃NO₂

Purity: Min. 95%

Color and Shape: Off-White Powder

Molecular weight: 251.28 g/mol

Ref: 3D-FB18516