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3-(5-methylfuran-2-yl)-3-oxopropanenitrile is a chemical compound with the molecular formula C8H7NO2. It is a derivative of propenenitrile, featuring a 5-methylfuran-2-yl group attached to the 3-position. 3-(5-methylfuran-2-yl)-3-oxopropanenitrile is characterized by its furan ring, which is a heterocyclic aromatic ring containing one oxygen atom, and a methyl group at the 5-position. The molecule also has a cyano group (-CN) at the 3-position, which is a nitrile functional group. 3-(5-methylfuran-2-yl)-3-oxopropanenitrile is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and other chemical products due to its unique structure and reactivity.

197250-40-1

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197250-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197250-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,2,5 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 197250-40:
(8*1)+(7*9)+(6*7)+(5*2)+(4*5)+(3*0)+(2*4)+(1*0)=151
151 % 10 = 1
So 197250-40-1 is a valid CAS Registry Number.

197250-40-1Downstream Products

197250-40-1Relevant academic research and scientific papers

Development of a continuous flow photoisomerization reaction converting isoxazoles into diverse oxazole products

Bracken, Cormac,Baumann, Marcus

, p. 2607 - 2617 (2020/03/11)

A continuous flow process is presented, which directly converts isoxazoles into their oxazole counterparts via a photochemical transposition reaction. This results in the first reported exploitation of this transformation to establish its scope and synthe

Simple Synthesis of 3-Oxopropanenitriles via Electrophilic Cyanoacetylation of Heterocycles with Mixed Anhydrides

Andicsovà-Eckstein, Anita,Kozma, Erika,Végh, Daniel

, p. 1945 - 1949 (2016/11/24)

A simple and efficient method for the synthesis of 3-oxopropanenitriles from variously substituted heterocyclic compounds via direct electrophilic cyanoacetylation is described. A series of heterocyclic 3-oxopropanenitriles (2a, 2b, 2c, 2d, 2e, 2f, 2g, 2h, 2i, 2j, 2k) have been synthesized using mixed anhydride (acetic or trifluoroacetic anhydride:cyanoacetic acid) in the presence of Mg(ClO4)2·2H2O as catalyst. This method can be extended also for the cyanoacetylation of electron poor aromatic compounds.

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