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1-(4,7-dihydro-7-(4-methoxyphenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

329796-14-7

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329796-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329796-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,7,9 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 329796-14:
(8*3)+(7*2)+(6*9)+(5*7)+(4*9)+(3*6)+(2*1)+(1*4)=187
187 % 10 = 7
So 329796-14-7 is a valid CAS Registry Number.

329796-14-7Downstream Products

329796-14-7Relevant academic research and scientific papers

Three-component uncatalyzed eco-friendly reactions for one-pot synthesis of 4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine derivatives

El Rady, Eman A.

, p. 869 - 875 (2014)

A three-component system of one-pot synthesis of [1,2,4]triazolo[1,5-a] pyrimidine derivatives using condensation of 1,3-dicarbonyl compounds, aldehydes, and 5-amino[1,2,4]triazole in ethanol without any catalyst was reported in high yields via simple, efficient, and environmentally friendly process. The method reported herein considered a green process; this method has significant advantages of simple workup procedure, excellent yield, minimal environmental pollution, and short reaction time over classical reported methods.

Alkylation of 6-C(O)R-7-aryl-5-methyl-4,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidines

Kolosov, Maksim A.,Shvets, Elena H.,Kulyk, Olesia G.,Orlov, Valeriy D.

, p. 1052 - 1056 (2016/08/26)

Alkylation of 6-C(O)R-7-aryl-5-methyl-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidines with methyl iodide or ethyl bromide in either saturated aqueous KOH–MeCN or NaH–DMF led to the formation of N4-alkyl derivatives in good yields (60–98%). Reactivity of the acetyl group of N4-alkyl derivatives towards aromatic aldehydes under the conditions of the Claisen–Schmidt reaction was significantly higher than in 4-unsubstituted compounds. The starting 6-C(O)R-7-aryl-5-methyl-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidines were synthesized via a three-component condensation of an aromatic aldehyde, 3-amino-1,2,4-triazole, and a dicarbonyl compound (2,4-pentanedione or ethyl acetoacetate) in DMF.

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