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2-Methyl-5-phenyl-1,3-dioxolan-4-one is a chemical compound with the molecular formula C10H10O3. It is a heterocyclic organic compound, specifically a dioxolanone derivative, featuring a dioxolane ring fused to a carbonyl group. 2-Methyl-5-phenyl-1,3-dioxolan-4-one is known for its potential applications in organic synthesis, particularly as a building block for the creation of more complex molecules. It is characterized by its unique structure, which includes a methyl group at the 2-position and a phenyl group at the 5-position of the dioxolane ring. The compound's properties, such as its reactivity and stability, can be influenced by the presence of these substituents, making it a valuable intermediate in the synthesis of various pharmaceuticals and other specialty chemicals.

6454-27-9

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6454-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6454-27-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6454-27:
(6*6)+(5*4)+(4*5)+(3*4)+(2*2)+(1*7)=99
99 % 10 = 9
So 6454-27-9 is a valid CAS Registry Number.

6454-27-9Relevant academic research and scientific papers

Stereoselective Protonation of Carbanions, 3. - 1,3-Dioxolan-4-ones and 1,3-Oxazolidine-4-ones: Syntheses and Diastereoselective Protonation of their Anions

Huenig, Siegfried,Keita, Yango,Peters, Karl,Schnering, Hans-Georg von

, p. 1495 - 1500 (2007/10/02)

Dioxolonanones 3 and oxazolidinones 4 are synthesized by different methods together with the silyl enol ether 3aSi.The configuration of their diastereomers is determined by (1)H-NMR spectroscopy and relative retention times (vpc), backed by a c

A new highly diastereoselective synthesis of 2,5-disubstituted-1,3-dioxolan-4-ones from α-hydroxyacids

Chapel,Greiner,Ortholand

, p. 1441 - 1442 (2007/10/02)

Reaction of α-hydroxyacids with acetals under weak acid catalysis gave the corresponding dioxolanones with a better diastereomeric ratio than the usual strong acid catalyzed synthesis from aldehydes.

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