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4,5-dimethoxyimidazolidine-2-one is a chemical compound with the molecular formula C5H10N2O3. It is a heterocyclic compound, specifically an imidazolidine derivative, featuring a five-membered ring with two nitrogen atoms and one oxygen atom. The compound is characterized by the presence of two methoxy groups (-OCH3) attached to the 4th and 5th carbon atoms of the imidazolidine ring, and a carbonyl group (C=O) at the 2nd position. 4,5-dimethoxyimidazolidine-2-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. Due to its reactivity and functional groups, 4,5-dimethoxyimidazolidine-2-one can participate in a range of chemical reactions, making it a valuable building block in the creation of more complex molecules.

3891-44-9

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3891-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3891-44-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3891-44:
(6*3)+(5*8)+(4*9)+(3*1)+(2*4)+(1*4)=109
109 % 10 = 9
So 3891-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O3/c1-9-3-4(10-2)7-5(8)6-3/h3-4H,1-2H3,(H2,6,7,8)

3891-44-9Downstream Products

3891-44-9Relevant academic research and scientific papers

Syntheses and antimicrobial activities of five-membered ring heterocycles coupled to indole moieties

Pereira, Elisabeth Rodrigues,Sancelme, Martine,Towa, Jean-Jacques,Prudhomme, Michelle,Martre, Anne-Marie,Mousset, Guy,Rapp, Maryse

, p. 380 - 385 (2007/10/03)

Indole-substituted oxazolidinones, oxazolones, pyrrolidinone, imidazolidinone and imidazolones were synthesized. Their inhibitory potencies towards protein kinase C and protein kinase A were determined and their in vitro activities against Streptomyces chartreusis, Streptomyces griseus, Bacillus cereus, Candida albicans and Escherichia coli were examined. The inhibition of Streptomyces sporulation observed for some of them could not be linked to in vitro protein kinase C inhibition. All proved inactive against C. albicans but three of them exhibited a marked activity towards E. coli. This effect extends to other Gram-negative bacteria.

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