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Methyl 6-phenylpyran-2-one-4-carboxylate is a chemical compound with the molecular formula C13H10O4. It is a derivative of pyran-2-one, featuring a phenyl group at the 6th position and a carboxylate group at the 4th position. methyl 6-phenylpyran-2-one-4-carboxylate is known for its potential applications in the synthesis of various organic compounds and pharmaceuticals, particularly in the development of novel drugs and agrochemicals. Its structure allows for a range of chemical reactions, making it a valuable intermediate in organic synthesis. The compound's properties, such as its reactivity and stability, are influenced by the presence of the phenyl and carboxylate groups, which can participate in a variety of chemical transformations.

3448-44-0

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3448-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3448-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,4 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3448-44:
(6*3)+(5*4)+(4*4)+(3*8)+(2*4)+(1*4)=90
90 % 10 = 0
So 3448-44-0 is a valid CAS Registry Number.

3448-44-0Downstream Products

3448-44-0Relevant academic research and scientific papers

Photoinduced intramolecular cyclopentanation vs photoprotolytic oxametathesis in polycyclic alkenes outfitted with conformationally constrained aroylmethyl chromophores

Valiulin, Roman A.,Arisco, Teresa M.,Kutateladze, Andrei G.

, p. 2012 - 2025 (2013)

Intramolecular photoinduced cyclizations are investigated in photoprecursors assembled in a modular fashion via a Diels-Alder reaction of acetylenic dienophiles with subsequent Michael additions of aromatic ketones to install a chromophore capable of initiating Paternò-Büchi cycloadditions or radical cyclization cascades. The protolytic oxametathesis in these systems allows for rapid access to novel polycyclic scaffolds decorated by formyl groups and carboxylates suitable for subsequent modifications. In conformationally constrained photoprecursors, a radical rearrangement takes place resulting in intramolecular 1,3-diradical cyclopentanation of the double bond.

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