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2-Ethyl-3-(2-phenylbutyrylamino)quinazolin-4(3H)-one is a complex organic compound belonging to the quinazolinone class. It features a quinazolinone core with a 2-ethyl substituent at the 2-position and a 2-phenylbutyrylamino group at the 3-position. 2-ethyl-3-(2-phenylbutyrylamino)quinazolin-4(3H)-one is characterized by its unique molecular structure, which consists of a fused pyridine and pyrimidine ring system, with the phenylbutyrylamino side chain providing additional complexity. It is likely to have specific applications in medicinal chemistry or as a precursor in the synthesis of other compounds, given its structural features.

6761-31-5

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6761-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6761-31-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,6 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6761-31:
(6*6)+(5*7)+(4*6)+(3*1)+(2*3)+(1*1)=105
105 % 10 = 5
So 6761-31-5 is a valid CAS Registry Number.

6761-31-5Downstream Products

6761-31-5Relevant academic research and scientific papers

Regioselective lithiation of chiral 3-acylamino-2-alkylquinazolin-4(3H)- ones: Application in synthesis

Smith, Keith,El-Hiti, Gamal A.,Abdel-Megeed, Mohamed F.

, p. 2121 - 2130 (2004)

Reaction of 3-amino-2-alkylquinazolin-4(3H)-ones with several chiral acid chlorides was found to be dependent on the molar proportions. When a 1:1 molar mixture was heated under reflux, the corresponding 3-(diacylamino)- derivatives were obtained in poor yields. However, when a 2:1 molar mixture was reacted in refluxing toluene, the 3-acylamino- derivatives were obtained in good yields based on the acid chloride. Lithiation of the 3-acylamino-2-alkyl-quinazolin- 4(3H)-ones was achieved by the use of lithium diisopropylamide (LDA) in anhydrous THF at -78°C and the reaction was regioselective at the carbon α to position 2 of the quinazolin-4(3H)-one moiety. The dilithio reagents thus obtained reacted with electrophiles to give the corresponding 2-substituted derivatives in very good yields. The NMR spectra of the products show the expected diastereotopism for all the CH2 groups and provide evidence for long-range asymmetric induction.

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