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3-Furanpropanoic acid, 2-methyl-, also known as 2-methyl-3-furanpropanoic acid, is an organic compound with the chemical formula C7H8O3. It is a derivative of furanpropanoic acid, featuring a methyl group attached to the second carbon atom of the furan ring. 3-Furanpropanoic acid, 2-methyl- is characterized by its unique structure, which includes a furan ring (a five-membered ring with one oxygen atom) and a propanoic acid chain (a three-carbon chain ending in a carboxylic acid group). 2-methyl-3-furanpropanoic acid is a versatile building block in organic synthesis and can be used in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its properties, such as reactivity and stability, make it a valuable intermediate in the synthesis of complex molecules.

5554-98-3

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5554-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5554-98-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5554-98:
(6*5)+(5*5)+(4*5)+(3*4)+(2*9)+(1*8)=113
113 % 10 = 3
So 5554-98-3 is a valid CAS Registry Number.

5554-98-3Downstream Products

5554-98-3Relevant academic research and scientific papers

131. Synthesis of 2-Cycloalkenones (Parts of 1,4-Diacyl-1,3-butadiene Systems) and of a Heterocyclic Analogue by Metal-Catalyzed Decomposition of 2-Diazoacylfurans

Wenkert, Ernest,Guo, Ming,Pizzo, Ferdinando,Ramachandran, Kishore

, p. 1429 - 1438 (2007/10/02)

Furans with side-chains at C(2) of various lengths terminating in diazomethyl keto groups are shown to undergo Rh2(OAc)4-catalyzed furan unravelling with the production of 2-cyclopentenone, 2-cyclohexenone, and 2-cycloheptenone to each of whose olefinic C(β) is attached an acrylaldehyde unit.Interposition of a cyclohexane or a methylaminomethylene moiety between the furan and diazoketo functions leads to the formation of a hydroindenone and pyrrolone, respectively.Replacement of the diazomethylketo terminus by an α-diazoethylketo system or a α-diazo-β-keto-ester function produces 2-substituted 2-cycloalkenones.A furan with a C4, diazomethylketo-terminating side-chain at C(3) is described to be transformed into a 4-formylmethylidene-2-cyclohexenone.

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