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233256-44-5

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233256-44-5 Usage

General Description

"(S)-2-(4,5-dihydro-4-phenyloxazol-2-yl)methylpyridine" is a chemical compound with a unique molecular structure. It contains 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 second carbon of the pyridine ring. The compound exists in a chiral form known as (S)-2-(4,5-dihydro-4-phenyloxazol-2-yl)methylpyridine, meaning it has a specific spatial arrangement of atoms that gives it distinct chemical properties. (S)-2-<<4,5-dihydro-4-phenyloxazol-2-yl>methyl>pyridine may have various applications in the field of pharmaceuticals or organic synthesis due to its unique structure and potentially useful properties.

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 articles and documents

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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