CAS 119-62-0

2-Amino-1-(4-nitrophenyl)-1,3-propanediol

Description:

2-Amino-1-(4-nitrophenyl)-1,3-propanediol, with the CAS number 119-62-0, is an organic compound characterized by its amino and nitro functional groups. It features a propanediol backbone, which contributes to its solubility in polar solvents. The presence of the 4-nitrophenyl group imparts significant electronic properties, making it a useful intermediate in organic synthesis and pharmaceuticals. This compound typically appears as a crystalline solid and exhibits moderate stability under standard conditions. Its amino group can participate in various chemical reactions, including acylation and alkylation, while the nitro group can undergo reduction to form amines. Additionally, 2-Amino-1-(4-nitrophenyl)-1,3-propanediol may exhibit biological activity, which has been explored in various research contexts. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, this compound serves as an important building block in the synthesis of more complex molecules in medicinal chemistry and materials science.

Formula: C₉H₁₂N₂O₄

InChI: InChI=1S/C9H12N2O4/c10-8(5-12)9(13)6-1-3-7(4-2-6)11(14)15/h1-4,8-9,12-13H,5,10H2

InChI key: InChIKey=OCYJXSUPZMNXEN-UHFFFAOYSA-N

SMILES: C(C(CO)N)(O)C1=CC=C(N(=O)=O)C=C1

Synonyms:

• DL-Aminodialcohol
• 2-Amino-1-(4-Nitrophenyl)-1,3-Propanediol
• 1,3-Propanediol, 2-amino-1-(4-nitrophenyl)-
• 1,3-Propanediol, 2-amino-1-(p-nitrophenyl)-
• 1-(p-Nitrophenyl)-2-amino-1,3-propanediol
• 2-Amino-1-(4-nitrophenyl)-1,3-propanediol
• 2-Amino-1-(4-nitrophenyl)-1,3-Propanediol (DL-)
• p-Nitrophenyl-2-amino-1,3-propanediol

1,3-Propanediol, 2-amino-1-(4-nitrophenyl)-

CAS: 119-62-0

Formula: C₉H₁₂N₂O₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 212.2026

Ref: IN-DA000P01

2-Amino-1-(4-nitrophenyl)-1,3-propanediol

CAS: 119-62-0

2-Amino-1-(4-nitrophenyl)-1,3-propanediol (2APPD) is a diagnostic reagent that can be used to identify tuberculosis infections. 2APPD is an acidic compound that can be synthesized by the reaction of 4-nitrophenol and formaldehyde. The absorbance of 2APPD at 400 nm can be measured using a colorimetric method. It has been shown that the initial rate of deaggregation of 2APPD depends on the pH and ionic strength of the environment. A schematic diagram illustrating this process is available in this article. Gold nanoparticles are uncharged and do not react with 2APPD, which makes them ideal for use in developing biosensors for detecting this compound.

Formula: C₉H₁₂N₂O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 212.2 g/mol

Ref: 3D-AAA11962

Chloramphenicol Impurity 2

CAS: 119-62-0

Formula: C₉H₁₂N₂O₄

Molecular weight: 212.2

Ref: ST-EA-CP-C161003