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3-(6-methoxynaphthalen-2-yl)propionic acid is a chemical compound with the molecular formula C12H12O3. It is a derivative of naphthalene, featuring a methoxy group at the 6-position and a propionic acid group at the 3-position. This organic molecule is known for its potential applications in the synthesis of pharmaceuticals and other chemical products. Its structure provides a foundation for further functionalization and can be used as a building block in the development of new compounds with specific properties. The compound's unique arrangement of atoms and functional groups may contribute to its reactivity and stability, making it a valuable component in various chemical processes.

3453-40-5

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3453-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3453-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3453-40:
(6*3)+(5*4)+(4*5)+(3*3)+(2*4)+(1*0)=75
75 % 10 = 5
So 3453-40-5 is a valid CAS Registry Number.

3453-40-5Relevant academic research and scientific papers

Highly active water-soluble palladium catalyst for the regioselective carbonylation of vinyl aromatics to 2-arylpropionic acids

Jayasree,Seayad,Chaudhari

, p. 1239 - 1240 (2007/10/03)

A novel water-soluble Pd complex containing pyridine carboxylate and TPPTS as ligands is a highly active catalyst for the carbonylation of vinyl aromatics under biphasic conditions and provides high regioselectivity to 2- arylpropionic acids.

Highly active supported palladium catalyst for the regioselective synthesis of 2-arylpropionic acids by carbonylation

Jayasree,Seayad,Chaudhari

, p. 1067 - 1068 (2007/10/03)

A catalyst system consisting of supported palladium in the presence of phosphine ligands, TsOH and LiCl catalyses the carbonylation of 1-arylethanols to 2-arylpropionic acids with significantly improved activity and regioselectivity; the catalyst can be recycled with no loss in activity and selectivity.

DIRECT, REGIOSELECTIVE HYDROCARBOXYLATION OF ALKYNES TO SATURATED ACIDS BY COBALT AND NICKEL CATALYSTS UNDER PHASE TRANSFER CONDITIONS

Lee, Jong-Tae,Alper, Howard

, p. 1769 - 1770 (2007/10/02)

Phase transfer catalyzed carbonylation of alkynes in the presence of cobalt chloride, potassium cyanide, and nickel cyanide affords saturated carboxylic acids, with good selectivity observed for the branched-chain isomer.

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