CAS 101860-83-7

1-(4-Bromo-3-nitrophenyl)-1-propanone

Description:

1-(4-Bromo-3-nitrophenyl)-1-propanone, with the CAS number 101860-83-7, is an organic compound characterized by its structure, which includes a propanone moiety attached to a phenyl ring that is substituted with both a bromine and a nitro group. This compound typically appears as a solid at room temperature and is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the bromine and nitro substituents contributes to its reactivity, making it a useful intermediate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic addition. Additionally, the compound's functional groups may impart specific physical properties, such as solubility in organic solvents and varying degrees of polarity. Safety precautions should be observed when handling this compound, as it may pose health risks due to its halogenated and nitro functionalities. Overall, 1-(4-Bromo-3-nitrophenyl)-1-propanone is a notable compound in the field of synthetic organic chemistry.

Formula: C₉H₈BrNO₃

InChI: InChI=1S/C9H8BrNO3/c1-2-9(12)6-3-4-7(10)8(5-6)11(13)14/h3-5H,2H2,1H3

InChI key: InChIKey=TZELZSUMAATQRO-UHFFFAOYSA-N

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

Synonyms:

• 1-(4-Bromo-3-Nitrophenyl)Propan-1-One
• 1-(4-Bromo-3-nitrophenyl)-1-propanone
• 1-Propanone, 1-(4-bromo-3-nitrophenyl)-
• Ns 123
• Propiophenone, 4′-bromo-3′-nitro-

1-(4-Bromo-3-nitrophenyl)propan-1-one

CAS: 101860-83-7

Formula: C₉H₈BrNO₃

Molecular weight: 258.0687

Ref: IN-DA008UMO

1-(4-Bromo-3-nitrophenyl)-1-propanone

CAS: 101860-83-7

1-(4-Bromo-3-nitrophenyl)-1-propanone

Formula: C₉H₈BrNO₃

Purity: 98%

Color and Shape: off white to faint yellow crystals

Molecular weight: 258.07g/mol

Ref: 54-OR450140

4'-Bromo-3'-nitropropiophenone

CAS: 101860-83-7

4'-Bromo-3'-nitropropiophenone (4BNPP) is a nitrophenol that has been shown to inhibit DNA repair. 4BNPP inhibits the synthesis of DNA by inhibiting the activity of topoisomerase II, which is an enzyme involved in the replication and repair of DNA. In addition, 4BNPP has been shown to have radiosensitizing properties and is used as a treatment for cancer. 4BNPP binds to human astrocytes and tissues, causing damage that may lead to cancerous cells. This drug also causes tumor regression in mice with prostate cancer cells and enhances radiation therapy for glioma and colorectal carcinoma cells.

Formula: C₉H₈BrNO₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 258.07 g/mol

Ref: 3D-FB70843