1705-09-5 Usage
General Description
2-MERCAPTO-3-METHYL-3H-QUINAZOLIN-4-ONE, also known as amtolmetin guacil, is a chemical compound with potential anti-inflammatory and analgesic properties. It is a non-steroidal anti-inflammatory drug (NSAID) that belongs to the class of quinazolinones. 2-MERCAPTO-3-METHYL-3H-QUINAZOLIN-4-ONE works by inhibiting the production of prostaglandins, which are responsible for causing pain and inflammation in the body. It is commonly used as a treatment for various types of pain and inflammation, including arthritis and menstrual cramps. Additionally, it has been studied for its potential anti-cancer effects, particularly in combination with other chemotherapeutic agents. However, it is important to note that this compound may have potential side effects and should be used under the guidance of a healthcare professional.
Check Digit Verification of cas no
The CAS Registry Mumber 1705-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1705-09:
(6*1)+(5*7)+(4*0)+(3*5)+(2*0)+(1*9)=65
65 % 10 = 5
So 1705-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2OS/c1-11-8(12)6-4-2-3-5-7(6)10-9(11)13/h2-5H,1H3,(H,10,13)
1705-09-5Relevant articles and documents
The Invention of New Radical Chain Reactions. Part 9. Further Radical Chemistry of Thiohydroxamic Esters; Formation of Carbon-Carbon Bonds
Barton, Derek H.R.,Crich, David,Kretzschmar, Gerhard
, p. 39 - 54 (2007/10/02)
Carbon radicals derived from the esters of several types of thiohydroxamic acids have been trapped in a number of different ways.Particular attention has been paid to carbon-carbon bond formation by addition to suitably activated ethylenic linkages.Carboxylic acids can be conveniently converted into homo- and bishomo-acids by free radical chemistry based on thiohydroxamic esters.In a coda the tautomerism of the thiohydroxamic acids have been examined by physical methods.It is confirmed that the esters used are derivatives of the thione tautomer.
SYNTHESIS AND ALKYLATION OF 2-MERCAPTO-4-QUINAZOLONE AND THE FUNGICIDAL ACTIVITIES OF THE COMPOUNDS OBTAINED
Shakhadoyatov, Kh. M.,Yangibaev, S.,Yun, L. M.,Kadyrov, Ch. Sh.
, p. 106 - 111 (2007/10/02)
A convenient method of obtaining 2-mercapto-4-quinazolone has been developed and the alkylation of its ambidentate anions has been studied.It has been found that they exhibit a dual reactivity in alkylation reactions.It has been shown that alkylated 2-mercapto-4-quinazolones possess a moderate fungicidal activity.
