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(S)-2-(4,5-dihydro-4-phenyloxazol-2-yl)methylpyridine is a chemical compound characterized by its unique molecular structure, featuring a pyridine ring with a methyl group attached to the second carbon atom, and a 4,5-dihydro-4-phenyloxazol-2-yl group attached to the same carbon. (S)-2-<<4,5-dihydro-4-phenyloxazol-2-yl>methyl>pyridine exists in a chiral form, known as (S)-2-(4,5-dihydro-4-phenyloxazol-2-yl)methylpyridine, which possesses a specific spatial arrangement of atoms that confers distinct chemical properties. Its structure and potential properties make it a candidate for various applications in the pharmaceutical and organic synthesis industries.

233256-44-5

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233256-44-5 Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-(4,5-dihydro-4-phenyloxazol-2-yl)methylpyridine is used as a key intermediate for the synthesis of various pharmaceutical compounds due to its unique molecular structure and potentially useful properties. Its specific spatial arrangement of atoms allows for the development of novel drugs with improved efficacy and selectivity.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-2-(4,5-dihydro-4-phenyloxazol-2-yl)methylpyridine serves as a valuable building block for the creation of complex organic molecules. Its unique structure can be utilized to synthesize a wide range of compounds with diverse applications, including pharmaceuticals, agrochemicals, and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 233256-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,2,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 233256-44:
(8*2)+(7*3)+(6*3)+(5*2)+(4*5)+(3*6)+(2*4)+(1*4)=115
115 % 10 = 5
So 233256-44-5 is a valid CAS Registry Number.

233256-44-5Downstream Products

233256-44-5Relevant academic research and scientific papers

Chiral pyridylmethyl- and quinolinyl-oxazolines as ligands for enantioselective palladium-catalyzed allylic alkylation

Chelucci, Giorgio,Gladiali, Serafino,Saba, Antonio

, p. 1393 - 1400 (2007/10/03)

Chiral pyridylmethyl- and quinolinyl-oxazolines were prepared and assessed in the enantioselective palladium-catalyzed allylic substitution of 1,3-diphenylprop-2-enyl acetate with dimethyl malonate. Enantioselectivities up to 77% were obtained.

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