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2-(allylthio)-3-(4-chlorophenyl)quinazolin-4(3H)-one is a complex organic compound belonging to the quinazolinone class, characterized by a quinazoline ring system with a 4(3H)-one functional group. 2-(allylthio)-3-(4-chlorophenyl)quinazolin-4(3H)-one features a 4-chlorophenyl group at the 3-position and an allylthio group at the 2-position, which contributes to its unique chemical properties. It is primarily used in the pharmaceutical industry as a potential drug candidate or as an intermediate in the synthesis of various biologically active molecules. Due to its specific structure, it may exhibit various biological activities, such as anti-inflammatory, analgesic, or anti-cancer properties, depending on its interaction with target proteins or enzymes. However, further research and testing are required to determine its exact therapeutic potential and safety profile.

1039-01-6

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1039-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1039-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1039-01:
(6*1)+(5*0)+(4*3)+(3*9)+(2*0)+(1*1)=46
46 % 10 = 6
So 1039-01-6 is a valid CAS Registry Number.

1039-01-6Downstream Products

1039-01-6Relevant academic research and scientific papers

Synthesis, molecular structure and spectroscopic studies of some new quinazolin-4(3H)-one derivatives; An account on the N- versus S-Alkylation

Hagar, Mohamed,Soliman, Saied M.,Ibid, Farahate,El Ashry, El Sayed H.

, p. 667 - 679 (2016)

A new series of N- and S-alkylated products of 3-aryl-1H,3H-quinazolin-2,4-dione and 3-aryl-2-mercapto-3H-quinazolin-4-one, respectively, were prepared in good yields via efficient nucleophilic substitution reaction of the SH and NH substrates with methyl

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