CAS 129722-34-5

7-(4-Bromobutoxy)-3,4-dihydro-2(1H)-quinolinone

Description:

7-(4-Bromobutoxy)-3,4-dihydro-2(1H)-quinolinone is a chemical compound characterized by its unique structure, which includes a quinolinone core modified with a bromobutoxy side chain. This compound features a bicyclic structure that contributes to its potential biological activity. The presence of the bromine atom enhances its reactivity and may influence its pharmacological properties. The butoxy group can affect solubility and lipophilicity, which are important for its interaction with biological membranes. This compound may exhibit various properties, including potential antimicrobial, anti-inflammatory, or anticancer activities, making it of interest in medicinal chemistry. Its molecular weight, melting point, and solubility characteristics would be relevant for applications in drug formulation and development. As with many organic compounds, safety data, including toxicity and handling precautions, should be consulted before use. Overall, 7-(4-Bromobutoxy)-3,4-dihydro-2(1H)-quinolinone represents a class of compounds that could be explored for therapeutic applications based on its structural features.

Formula: C₁₃H₁₆BrNO₂

InChI: InChI=1S/C13H16BrNO2/c14-7-1-2-8-17-11-5-3-10-4-6-13(16)15-12(10)9-11/h3,5,9H,1-2,4,6-8H2,(H,15,16)

InChI key: InChIKey=URHLNHVYMNBPEO-UHFFFAOYSA-N

SMILES: O(CCCCBr)C=1C=C2C(=CC1)CCC(=O)N2

Synonyms:

• 2(1H)-Quinolinone, 7-(4-bromobutoxy)-3,4-dihydro-
• 3,4-Dihydro-7-(4-Bromobutoxy)-2(1H)-Quinolinone
• 3,4-Dihydro-7-(4-bromo butoxy)-2(1H)-quinolinone
• 7-(3-bromopropoxy)-3,4-dihydro-1H-quinolin-2-one
• 7-(4-Bromobutoxy)-1,2,3,4-tetrahydroquinoline-2-one
• 7-(4-Bromobutoxy)-2(1H)-3,4-Dihydroquinolinone
• 7-(4-Bromobutoxy)-3,4-Dihydro-2-Quinolinone
• 7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one
• 7-(4-Bromobutoxy)-3,4-dihydroquinoline-2(1H)-one
• 7-(4-Bromobutoxy)3,4-dihyrdro-2(H)-Quinolinone
• 7-(4-bromo-butoxy)-3,4-dihydro-1H-quinolin-2-one
• 7-(4-bromobutoxy)-3,4-dihydroquinolin-2(1H)-one
• 7-hydroxy-(4-Bromobutyloxy)-2(1H)-3,4-dihydroquinolinone
• Lanzapine

7-(4-Bromobutoxy)-3,4-dihydro-2(1H)-quinolinone

CAS: 129722-34-5

Formula: C₁₃H₁₆BrNO₂

Purity: >98.0%(HPLC)(N)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 298.18

Ref: 3B-B3333

3,4-Dihydro-7-(4-bromobutoxy)-2(1h)-quinolinone

CAS: 129722-34-5

Formula: C₁₃H₁₆BrNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 298.1756

Ref: IN-DA000TMD

Aripiprazole Impurity 29

CAS: 129722-34-5

Formula: C₁₃H₁₆BrNO₂

Color and Shape: White To Off-White Solid

Molecular weight: 298.18

Ref: 4Z-A-1453

7-(4-Bromobutoxy)-3,4-dihydro-2(1H)-quinolinone

Controlled Product

CAS: 129722-34-5

Formula: C₁₃H₁₆BrNO₂

Color and Shape: Neat

Molecular weight: 298.18

Ref: 86-MM0961.09

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2(1H)-one

CAS: 129722-34-5

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2(1H)-one

Purity: 98%

Color and Shape: Powder

Molecular weight: 298.18g/mol

Ref: 54-OR61174

Aripiprazole Bromobutoxyquinoline Impurity

CAS: 129722-34-5

Formula: C₁₃H₁₆BrNO₂

Molecular weight: 298.18

Ref: ST-EA-CP-A22009

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one

Controlled Product

CAS: 129722-34-5

Impurity Aripiprazole Bromobutoxyquinoline Impurity
Stability Hygroscopic
Applications An impurity in the synthesis of Aripiprazole (A771000). A degradation product in Aripiprazole tablets. Aripiprazole Bromobutoxyquinoline Impurity
References Reddy, G.V.R., et al.: Eur. J. Chem., 1, 20 (2010),

Formula: C₁₃H₁₆BrNO₂

Color and Shape: White To Off-White

Molecular weight: 298.18

Ref: TR-B681960

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one

CAS: 129722-34-5

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one is a palladium catalyst that can be used in a Buchwald reaction. This reaction is an industrially scalable process that has been developed to produce high yields of valuable organic compounds from inexpensive starting materials. The catalytic cycle involves the formation of the palladium species Pd(0) followed by its oxidative addition to an alkyl halide. This addition leads to the formation of a palladium(II) species and subsequent reductive elimination of hydrogen halide. 7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one is used as a catalyst in this process because it selectively reacts with electron rich aromatic substrates to form substituted benzoquinones or phenols. The product distribution is determined by the reactivity of the substrate and the relative rates of competing reactions. Impurities are formed during synthesis due to

Formula: C₁₃H₁₆BrNO₂

Purity: Min. 95%

Molecular weight: 298.18 g/mol

Ref: 3D-FB19204

7-(4-Bromo-butoxy)-3,4-dihydro-1H-quinolin-2-one

CAS: 129722-34-5

Formula: C₁₃H₁₆BrNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 298.18

Ref: 10-F048732

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2(1H)-one

CAS: 129722-34-5

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2(1H)-one is a useful organic compound for research related to life sciences. The catalog number is T65919 and the CAS number is 129722-34-5.

Formula: C₁₃H₁₆BrNO₂

Color and Shape: Solid

Molecular weight: 298.18

Ref: TM-T65919