CAS 1834-91-9

Ethanone, 1-(2-hydroxy-4-nitrophenyl)-

Description:

Ethanone, 1-(2-hydroxy-4-nitrophenyl)-, also known as 2-hydroxy-4-nitroacetophenone, is an organic compound characterized by its functional groups, including a ketone and a phenolic hydroxyl group. It features a nitro group attached to the aromatic ring, which contributes to its reactivity and potential applications in various chemical processes. This compound typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its aromatic nature. The presence of the hydroxyl group enhances its ability to participate in hydrogen bonding, influencing its solubility and reactivity. Its nitro substituent can also affect the electronic properties of the molecule, making it useful in synthetic organic chemistry, particularly in the development of dyes, pharmaceuticals, and agrochemicals. Safety data indicates that, like many nitro compounds, it should be handled with care due to potential toxicity and environmental impact. Proper storage and handling protocols are essential to mitigate risks associated with exposure.

Formula: C₈H₇NO₄

Ethanone, 1-(2-hydroxy-4-nitrophenyl)-

CAS: 1834-91-9

Formula: C₈H₇NO₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 181.1455

Ref: IN-DA0027KF

1-(2-Hydroxy-4-nitrophenyl)ethan-1-one

CAS: 1834-91-9

1-(2-Hydroxy-4-nitrophenyl)ethan-1-one

Purity: ≥95%

Molecular weight: 181.15g/mol

Ref: 54-OR22396

1-(2-Hydroxy-4-nitrophenyl)ethanone

CAS: 1834-91-9

Purity: 95%

Molecular weight: 181.1470032

Ref: 10-F759759

1-(2-Hydroxy-4-nitrophenyl)ethan-1-one

CAS: 1834-91-9

1-(2-Hydroxy-4-nitrophenyl)ethan-1-one (KPNE) is a potassium salt of a diketone that has antitubercular activity. KPNE inhibits the growth of Mycobacterium tuberculosis and has been shown to be effective as an antitubercular agent in animals. KPNE also has antiviral properties, inhibiting the RNA polymerase in HIV, which may be due to its ability to inhibit the synthesis of DNA. The mechanism of action for KPNE is thought to be due to its hydrolysis into 4-aminosalicylic acid, which inhibits bacterial protein synthesis by inhibition of the enzyme dihydrofolate reductase.

Formula: C₈H₇NO₄

Purity: Min. 95%

Molecular weight: 181.15 g/mol

Ref: 3D-BAA83491