CAS 6531-13-1

1-(4-nitrophenyl)ethanol

Description:

1-(4-Nitrophenyl)ethanol, with the CAS number 6531-13-1, is an organic compound characterized by the presence of a hydroxyl group (-OH) attached to an ethyl group, which is further substituted with a para-nitrophenyl group. This compound typically appears as a solid or crystalline substance and is known for its yellow color due to the nitro group. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. The presence of the nitro group imparts significant electron-withdrawing properties, influencing the compound's reactivity and making it a useful intermediate in organic synthesis. 1-(4-Nitrophenyl)ethanol can participate in various chemical reactions, including nucleophilic substitutions and reductions. Additionally, it may exhibit biological activity, making it of interest in pharmaceutical research. Safety precautions should be taken when handling this compound, as nitro compounds can be hazardous. Overall, its unique structure and properties make it a valuable compound in both industrial and research applications.

Formula: C₈H₈NO₃

InChI: InChI=1/C8H9NO3/c1-6(10)7-2-4-8(5-3-7)9(11)12/h2-6,10H,1H3

SMILES: CC(c1ccc(cc1)N(=O)=O)O

Synonyms:

• Benzenemethanol, .alpha.-methyl-4-nitro-

1-(4-Nitrophenyl)ethanol

CAS: 6531-13-1

Formula: C₈H₉NO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 167.1620

Ref: IN-DA00E93K

1-(4-Nitrophenyl)ethan-1-ol

CAS: 6531-13-1

1-(4-Nitrophenyl)ethan-1-ol

Purity: 98%

Molecular weight: 167.16g/mol

Ref: 54-OR74158

4-Nitrophenylmethylcarbinol

CAS: 6531-13-1

4-Nitrophenylmethylcarbinol is a nitro compound that has been isolated from the nitration of 4-nitrophenol. It is used as a reagent to synthesize β-unsaturated ketones. The inhibitory effect of 4-nitrophenylmethylcarbinol is due to the presence of two nitro groups and one methyl group on its structure. This compound has been shown to have an inhibitory effect on glucose 6-phosphate dehydrogenase, which functions in cellular respiration by catalyzing the conversion of glucose 6-phosphate to glucose 1,6-bisphosphate. The inhibition of this enzyme leads to a reduction in the formation of ATP and NADPH, which are essential for cell growth. 4-Nitrophenylmethylcarbinol also has reductase activities that allow it to reduce phosphotriesters (e.g., DNA) and dehydrogenase deficiency (e.g., py

Formula: C₈H₉NO₃

Purity: Min. 95%

Color and Shape: Orange Clear Liquid

Molecular weight: 167.16 g/mol

Ref: 3D-FN67326

1-(4-nitrophenyl)ethanol

CAS: 6531-13-1

Formula: C₈H₉NO₃

Purity: 98%

Color and Shape: Low Melting Solid

Molecular weight: 167.164

Ref: 10-F373534

1-(4-Nitrophenyl)ethanol

Controlled Product

CAS: 6531-13-1

Applications 1-(4-Nitrophenyl)ethanol (cas# 6531-13-1) is a useful research chemical.

Formula: C₈H₉NO₃

Color and Shape: Neat

Molecular weight: 167.16

Ref: TR-N545403