CAS 3156-44-3

3-(2-Nitroethenyl)phenol

Description:

3-(2-Nitroethenyl)phenol, with the CAS number 3156-44-3, is an organic compound characterized by the presence of a phenolic group and a nitroethenyl substituent. This compound features a nitro group (-NO2) attached to a vinyl group (-CH=CH2), which is further connected to a phenolic ring. The presence of the nitro group imparts significant electron-withdrawing properties, influencing the compound's reactivity and stability. Typically, compounds like 3-(2-Nitroethenyl)phenol exhibit properties such as moderate solubility in organic solvents and potential applications in organic synthesis, particularly in the development of dyes, pharmaceuticals, or agrochemicals. The phenolic hydroxyl group can participate in hydrogen bonding, affecting the compound's physical properties, such as melting and boiling points. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. However, handling and usage should be approached with caution due to the potential toxicity associated with nitro compounds.

Formula: C₈H₇NO₃

InChI: InChI=1S/C8H7NO3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H

InChI key: InChIKey=DHTXBJQMDPODIB-UHFFFAOYSA-N

SMILES: C(=CN(=O)=O)C1=CC(O)=CC=C1

Synonyms:

• 3-(2-Nitroethenyl)phenol
• 3-Hydroxy-β-nitrostyrene
• 3-[(E)-2-Nitrovinyl]phenol
• Phenol, 3-(2-nitroethenyl)-
• Phenol, 3-[(E)-2-nitroethenyl]-
• Phenol, m-(2-nitrovinyl)-

trans-3-Hydroxy-β-nitrostyrene

CAS: 3156-44-3

Formula: C₈H₇NO₃

Molecular weight: 165.1461

Ref: IN-DA003UXE

1-(3-Hydroxyphenyl)-2-nitroethene

CAS: 3156-44-3

1-(3-Hydroxyphenyl)-2-nitroethene

Purity: 95%

Molecular weight: 165.15g/mol

Ref: 54-OR957830

1-(3-Hydroxyphenyl)-2-nitroethene

CAS: 3156-44-3

1-(3-Hydroxyphenyl)-2-nitroethene is an organocatalytic chiral catalyst that has been shown to catalyze the asymmetric synthesis of a variety of organic compounds. The synthesis proceeds in two sequential steps: first, the enantioselective addition of nitroethane to a chiral thiourea followed by lactonization with quinine. This is an example of an asymmetric catalytic process.

Formula: C₈H₇NO₃

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 165.15 g/mol

Ref: 3D-FH67893