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Pyridine, 2,6-dimethyl-3-phenyl-, also known as 2,6-dimethyl-3-phenylpyridine, is an organic compound with the chemical formula C12H13N. It is a derivative of pyridine, a heterocyclic aromatic compound containing a nitrogen atom in a six-membered ring. The molecule features two methyl groups at the 2nd and 6th positions and a phenyl group attached to the 3rd position. Pyridine, 2,6-dimethyl-3-phenyl- is a colorless to pale yellow liquid with a strong, characteristic odor. It is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. The compound is also known for its potential applications in materials science and as a ligand in coordination chemistry.

1463-03-2

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1463-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1463-03-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1463-03:
(6*1)+(5*4)+(4*6)+(3*3)+(2*0)+(1*3)=62
62 % 10 = 2
So 1463-03-2 is a valid CAS Registry Number.

1463-03-2Downstream Products

1463-03-2Relevant academic research and scientific papers

Double decarboxylative Claisen rearrangement reactions: Microwave-assisted de novo synthesis of pyridines

Craig, Donald,Paina, Federica,Smith, Stephen C.

supporting information; experimental part, p. 3408 - 3410 (2009/02/05)

Microwave-assisted double decarboxylative Claisen rearrangement of bis(allyl) 2-tosylmalonates provides substituted 1,6-heptadienes, which may be alkylated, and then converted into pyridines by ozonolysis followed by reaction with ammonia generated in sit

A Suzuki-Miyaura approach to a series of forensically relevant pyridines

Blachut, Dariusz,Czarnocki, Zbigniew,Wojtasiewicz, Krystyna

, p. 2855 - 2864 (2008/02/07)

A convenient and general method for the preparation of sixteen 3,5-diarylsubstituted 2,4- and 2,6-dimethylpyridines of high forensic importance is described. The Suzuki cross-coupling reaction between a range of ring-substituted phenylboronic acids and 3,

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