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3-(4-chlorophenyl)-2-[(4,5-dihydro-1H-imidazol-2-ylsulfanyl)methyl]quinazolin-4(3H)-one hydrobromide (1:1) is a complex organic compound with a molecular formula of C19H15BrClN4OS. It is a derivative of quinazolinone, a heterocyclic compound with potential applications in pharmaceuticals and medicinal chemistry. The structure features a quinazolinone core, a 4-chlorophenyl group, an imidazol-2-ylsulfanylmethyl side chain, and a hydrobromide ion. 3-(4-chlorophenyl)-2-[(4,5-dihydro-1H-imidazol-2-ylsulfanyl)methyl]quinazolin-4(3H)-one hydrobromide (1:1) is known for its potential biological activities, such as anti-inflammatory and anti-cancer properties, and is often studied for its interactions with various biological targets. The hydrobromide salt form indicates that it is a salt derived from the parent compound and hydrobromic acid, which can affect its solubility and stability in different environments.

61555-07-5

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61555-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61555-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,5 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61555-07:
(7*6)+(6*1)+(5*5)+(4*5)+(3*5)+(2*0)+(1*7)=115
115 % 10 = 5
So 61555-07-5 is a valid CAS Registry Number.

61555-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenyl)-2-(4,5-dihydro-1H-imidazol-2-ylsulfanylmethyl)quinazolin-4-one,hydrobromide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:61555-07-5 SDS

61555-07-5Upstream product

61555-07-5Downstream Products

61555-07-5Relevant academic research and scientific papers

Synthesis and central nervous system activity of quinazolones related to 2 methyl 3 (o tolyl) 4 (3H) quinazolone (methaqualone)

Ager,Harrison,Kennewell,Taylor

, p. 379 - 386 (2007/10/08)

A number of derivatives of 2-methyl-3-(o-tolyl)-4(3H)-quinazolone bearing new substituents on the 2-methyl group have been synthesized. It was established that most substitutions at this position reduce or remove the CNS depressant activity of methaqualone. From the series prepared only the 2-fluoromethyl derivative or certain isothiouronium salts, which could be hydrolyzed in vivo to the 2-mercaptomethyl derivative, showed activity of the same magnitude as methaqualone.

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