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95216-42-5

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95216-42-5 Usage

Description

1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one is a chemical compound with the molecular formula C17H13ClN2O. It is a quinazolinone derivative featuring a cyclobutyl substituent and a chlorophenyl group. 1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one exhibits a range of potential pharmacological activities, such as antiviral, antimicrobial, and antitumor properties, along with possible anti-inflammatory and analgesic effects. Ongoing research suggests its potential use in the development of new pharmaceuticals for various medical conditions.

Uses

Used in Pharmaceutical Industry:
1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one is used as a compound with potential applications in the development of new pharmaceuticals due to its antiviral, antimicrobial, and antitumor properties. Its diverse pharmacological activities make it a promising candidate for treating a variety of medical conditions.
Used in Antiviral Applications:
In the field of antiviral research, 1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one is used as an active compound for the development of new antiviral drugs, targeting a range of viral infections.
Used in Antimicrobial Applications:
1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one is utilized as an antimicrobial agent, potentially effective against various bacteria and other microorganisms, contributing to the development of new antibiotics and antifungal medications.
Used in Antitumor Applications:
Within the oncology sector, 1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one is used as a compound with antitumor properties, potentially aiding in the development of novel cancer treatments.
Used in Anti-inflammatory and Analgesic Applications:
1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one is also used as a compound with potential anti-inflammatory and analgesic effects, which could lead to the creation of new medications for pain relief and inflammation management.

Check Digit Verification of cas no

The CAS Registry Mumber 95216-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,1 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95216-42:
(7*9)+(6*5)+(5*2)+(4*1)+(3*6)+(2*4)+(1*2)=135
135 % 10 = 5
So 95216-42-5 is a valid CAS Registry Number.

95216-42-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4(1H)-Quinazolinone, 1-(4-chlorophenyl)-2-cyclobutyl-

1.2 Other means of identification

Product number -
Other names 1-(4-Chlorophenyl)-2-cyclobutylquinazolin-4(1H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:95216-42-5 SDS

95216-42-5Downstream Products

95216-42-5Relevant articles and documents

Studies on 4(1H)-quinazolinones. 5. Synthesis and antiinflammatory activity of 4(1H)-quinazolinone derivatives

Ozaki,Yamada,Oine,Ishizuka,Iwasawa

, p. 568 - 576 (2007/10/02)

A number of new 4(1H)-quinazolinones were synthesized and evaluated in the carrageenin-induced paw edema test. Most of the compounds were obtained by the cyclization of the appropriately substituted anthranilamides with acid chlorides, followed by further chemical transformation. Structure-activity data suggest that 2-isopropyl-1-phenyl-, 2-cyclopropyl-1-phenyl-, and 1-isopropyl-2-phenyl-4(1H)-quinazolinones afford optimal potency and the presence of a halogen atom is preferred for activity. Adrenalectomy does not affect the antiinflammatory test results. The best result taking into account both efficacy and side effects was displayed by 1-isoproyl-(2-fluorophenyl)-4(1H)-quinazolinone.

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