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(Z)-3-((benzylamino)methylene)dihydrofuran-2(3H)-one is a complex organic compound characterized by a dihydrofuran-2(3H)-one core structure, which features a five-membered furan ring fused with a dihydrofuran ring. The molecule is further defined by a (Z)-configuration, indicating the geometric arrangement of the double bond, with the benzylamino group attached to the methylene bridge. (Z)-3-((benzylamino)methylene)dihydrofuran-2(3H)-one is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and reactivity.

81326-86-5

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81326-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81326-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81326-86:
(7*8)+(6*1)+(5*3)+(4*2)+(3*6)+(2*8)+(1*6)=125
125 % 10 = 5
So 81326-86-5 is a valid CAS Registry Number.

81326-86-5Downstream Products

81326-86-5Relevant academic research and scientific papers

A Method for the Preparation of β-Amino-α,β-unsaturated Carbonyl Compounds: Study of Solvent Effect and Mechanism

R. S., Reyno,Sugunan, Akash,S., Ranganayakulu,Suresh, Cherumuttathu H.,Rajendar, Goreti

supporting information, p. 1040 - 1045 (2020/02/15)

An efficient method for the preparation of β-amino-α,β-unsaturated carbonyl compounds is demonstrated. Bench-stable sodium 3-oxo-enolates were prepared from carbonyl compounds, and reacted with amines in the presence of an acid and a desiccant. DFT studie

ENAMINOCARBONYL COMPOUNDS AND THEIR USE

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Page/Page column 12; 13, (2010/08/09)

The present invention relates to enaminocarbonyl compounds with the formula I, in which X denotes O or CH2, Y denotes N and each of R1 and R2 denotes hydrogen, or Y denotes a CH and either R1 or R2 denotes a C1-4 alkyl, and the remaining R1 or R2 denotes hydrogen, selected (for Y denoting CH and R1 or R2 denoting a C1-4 alkyl) from a group encompassing a mixture of R and S enantiomers enriched in either enantiomer R or enantiomer S, enantiomer R and enantiomer S. The present invention also relates to the use of compounds with the formula I, in which X denotes O or CH2, Y denotes a CH and either R1 or R2 is selected from a group encompassing hydrogen and a C1-4 alkyl, and the remaining R1 or R2 denotes hydrogen, for the modification of the taste of a product and/or preparation for oral administration.

Synthesis of furo[3,2-c]pyridine and furo[2,3-d]pyrimidine derivatives from butyrolactone diethylacetal

Marchenko,Granik

, p. 58 - 61 (2007/10/02)

The reaction of butyrolactone acetal with CH acids was used to synthesize 2-methylenetetrahydrofuran derivatives. The latter react with dimethylformimide acetal to give a dieneamine that is capable of undergoing cyclization to furo [3,2-c]pyrimidine derivatives. This two-ring system was also synthesized by the reaction of cyanacetamide with 3-dimethylaminomethylenebutyrolactone acetal. The indicated acetal can also react with amidine components to give furo [2,3-d]pyrimidine derivatives.

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