CAS 704-13-2

3-hydroxy-4-nitrobenzaldehyde

Description:

3-Hydroxy-4-nitrobenzaldehyde, with the CAS number 704-13-2, is an organic compound that features both hydroxyl and nitro functional groups attached to a benzaldehyde structure. This compound is characterized by its aromatic ring, which contributes to its stability and reactivity. The presence of the hydroxyl (-OH) group provides it with polar characteristics, enhancing its solubility in polar solvents, while the nitro (-NO2) group is known for its electron-withdrawing properties, influencing the compound's reactivity in electrophilic aromatic substitution reactions. Typically, 3-hydroxy-4-nitrobenzaldehyde appears as a yellow to orange crystalline solid and may exhibit a distinct odor. It is often used in organic synthesis and as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. Additionally, the compound may display biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled.

Formula: C₇H₅NO₄

InChI: InChI=1/C7H5NO4/c9-4-5-1-2-6(8(11)12)7(10)3-5/h1-4,10H

InChI key: InChIKey=AUBBVPIQUDFRQI-UHFFFAOYSA-N

SMILES: c1cc(c(cc1C=O)O)N(=O)=O

3-Hydroxy-4-nitrobenzaldehyde

CAS: 704-13-2

Formula: C₇H₅NO₄

Purity: >97.0%(GC)(T)

Color and Shape: Light yellow to Yellow to Green powder to crystal

Molecular weight: 167.12

Ref: 3B-H1334

Benzaldehyde, 3-​hydroxy-​4-​nitro-

CAS: 704-13-2

Formula: C₇H₅NO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 167.1189

Ref: IN-DA005V64

3-Hydroxy-4-nitrobenzaldehyde

CAS: 704-13-2

3-Hydroxy-4-nitrobenzaldehyde

Purity: 98%

Color and Shape: Solid

Molecular weight: 167.12g/mol

Ref: 54-OR72101

3-Hydroxy-4-Nitrobenzaldehyde

CAS: 704-13-2

Formula: C₇H₅NO₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 167.12

Ref: 10-F079049

3-Hydroxy-4-nitrobenzaldehyde

CAS: 704-13-2

3-Hydroxy-4-nitrobenzaldehyde is a ternary complex, which consists of three molecules that are bound to each other in a specific way. It has been observed in the nmr spectra and it has been proposed as a fluorescence probe for the detection of hydrogen bonds. 3-Hydroxy-4-nitrobenzaldehyde catalyzes the reaction by forming a covalent bond with the pbr322 dna, which is an important DNA molecule in bacteria. The enzyme mechanism is not fully understood, but it has been shown that it can bind to Toll-like receptor 4 (TLR4), which is an innate immune system protein. This binding event activates TLR4, leading to the inflammatory response. 3-Hydroxy-4-nitrobenzaldehyde has shown efficacy against microglia cells and animal experiments have shown that this compound may be useful for reducing pain after surgery or injury.

Formula: C₇H₅NO₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 167.12 g/mol

Ref: 3D-FH67250