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1H-Indene-1,3(2H)-dione, 2-(4-ethylphenyl)-, also known as 2-(4-ethylphenyl)-1H-indene-1,3(2H)-dione, is an organic compound with the molecular formula C16H14O2. It is a derivative of indene, a tricyclic aromatic hydrocarbon, with a carbonyl group at positions 1 and 3, and a 4-ethylphenyl group attached at the 2-position. 1H-Indene-1,3(2H)-dione, 2-(4-ethylphenyl)- is characterized by its unique molecular structure, which contributes to its chemical properties and potential applications in various fields, such as pharmaceuticals, materials science, and organic synthesis. The presence of the carbonyl groups and the aromatic ring system in the molecule endows it with reactivity and stability, making it a subject of interest for further research and development.

7561-67-3

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7561-67-3 Usage

Purpose

Treatment of high blood pressure and angina (chest pain)

Drug Class

Calcium channel blockers

Mechanism

Relaxing and widening blood vessels for easier blood flow and lowered blood pressure

Prescription Type

Long-term treatment

Form

Extended-release tablet

Dosage

Follow prescribed dosage and instructions

Common Side Effects

Flushing, dizziness, headache, and swelling in lower extremities

Serious Side Effects

Fast or irregular heartbeat, fainting, or difficulty breathing (requires immediate reporting to healthcare provider)

Check Digit Verification of cas no

The CAS Registry Mumber 7561-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,6 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7561-67:
(6*7)+(5*5)+(4*6)+(3*1)+(2*6)+(1*7)=113
113 % 10 = 3
So 7561-67-3 is a valid CAS Registry Number.

7561-67-3Downstream Products

7561-67-3Relevant academic research and scientific papers

Efficient and convenient synthesis, characterization, and antimicrobial evaluation of some new tetracyclic 1,4-benzothiazines

Mor, Satbir,Nagoria, Savita

, p. 169 - 178 (2016/02/23)

In the present study, 20 new tetracyclic 1,4-benzothiazines (4a-4 t) were conveniently synthesized in good yields and characterized by different spectral and physical techniques. The in vitro antimicrobial evaluation of the synthesized benzothiazine derivatives was performed by serial dilution against two Gram-positive bacteria [Bacillus subtilis (MTCC 441) and Staphylococcus epidermidis (MTCC 6880)], two Gram-negative bacteria [Escherichia coli (MTCC 1652) and Pseudomonas aeruginosa (MTCC 424)], and two fungal strains [Candida albicans (MTCC 227) and Aspergillus Niger (MTCC 8189)]. The derivatives 4 l and 4 t were found to be more potent than standard drug, i.e., fluconazole, against A. Niger and C. albicans, respectively.

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