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4(3H)-Quinazolinone, 2-(1-methylethyl)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32700-64-4

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32700-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32700-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,0 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32700-64:
(7*3)+(6*2)+(5*7)+(4*0)+(3*0)+(2*6)+(1*4)=84
84 % 10 = 4
So 32700-64-4 is a valid CAS Registry Number.

32700-64-4Downstream Products

32700-64-4Relevant academic research and scientific papers

Syntheses of quinazolinones from 2-iodobenzamides and enaminones via copper-catalyzed domino reactions

Songsichan, Teerawat,Promsuk, Jaturong,Rukachaisirikul, Vatcharin,Kaeobamrung, Juthanat

, p. 4571 - 4575 (2014/06/24)

N-Substituted 2-iodobenzamides and enaminones undergo cascade transformations to achieve quinazolinones via a copper-catalyzed Ullmann-type coupling, a Michael addition and a retro-Mannich reaction. A unique stereochemical feature of this domino process was that Z-enaminones reacted without external ligands, whereas E-enaminones required the assistance of ligands. This journal is

Amine-induced rearrangement of 4-imino-4H-3,1-benzoxazines to 4-quinazolinones via amidine carboxamides

Snider, Barry B.,Zeng, Hongbo

, p. 173 - 182 (2007/10/03)

Iminobenzoxazines (2) react with pyrrolidine in EtOAc at reflux to give amidine carboxamides (11), which cyclize to quinazolinones (3) on heating in 99:1 MeCN/HOAc. However, both amidines (11d) and (13d) are formed if R 1 = Ar and R2

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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