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(1Z,3Z)-1,3-bis[(S)-4-phenyl-4,5-dihydrooxazol-2-yl]methyleneisoindoline is a bisoxazoline-based ligand with the molecular formula C32H26N2O2. It features two oxazoline rings and an isoindoline backbone, which can coordinate to metal ions to form stable complexes. (1Z,3Z)-1,3-bis[(S)-4-phenyl-4,5-dihydrooxazol-2-yl]methyleneisoindoline is widely used in coordination chemistry and catalysis due to its unique structural features and ability to form stable metal complexes, making it a valuable tool in organic synthesis and catalysis.

1358991-52-2

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1358991-52-2 Usage

Uses

Used in Coordination Chemistry:
(1Z,3Z)-1,3-bis[(S)-4-phenyl-4,5-dihydrooxazol-2-yl]methyleneisoindoline is used as a ligand in coordination chemistry for its ability to coordinate with metal ions and form stable complexes. This property allows it to be employed in the development of new metal complexes with potential applications in various fields.
Used in Catalysis:
In the field of catalysis, (1Z,3Z)-1,3-bis[(S)-4-phenyl-4,5-dihydrooxazol-2-yl]methyleneisoindoline is used as a ligand to create metal complexes that act as catalysts in various organic transformations. Its unique structural features contribute to the efficiency and selectivity of these catalytic processes.
Used in Asymmetric Synthesis:
(1Z,3Z)-1,3-bis[(S)-4-phenyl-4,5-dihydrooxazol-2-yl]methyleneisoindoline is utilized as a chiral ligand in asymmetric synthesis for the production of enantiomerically pure compounds. (1Z,3Z)-1,3-bis[(S)-4-phenyl-4,5-dihydrooxazol-2-yl]methyleneisoindoline's ability to form stable metal complexes aids in the selective formation of desired chiral products, which is crucial in the synthesis of pharmaceuticals and other biologically active molecules.
Used in Organic Synthesis:
In organic synthesis, (1Z,3Z)-1,3-bis[(S)-4-phenyl-4,5-dihydrooxazol-2-yl]methyleneisoindoline is used as a ligand to facilitate various organic transformations. Its coordination to metal ions and the stability of the resulting complexes make it a valuable tool for enhancing the efficiency and selectivity of synthetic reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1358991-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,8,9,9 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1358991-52:
(9*1)+(8*3)+(7*5)+(6*8)+(5*9)+(4*9)+(3*1)+(2*5)+(1*2)=212
212 % 10 = 2
So 1358991-52-2 is a valid CAS Registry Number.

1358991-52-2Downstream Products

1358991-52-2Relevant academic research and scientific papers

The synthesis of a new class of chiral pincer ligands and their applications in enantioselective catalytic fluorinations and the Nozaki-Hiyama-Kishi reaction

Deng, Qing-Hai,Wadepohl, Hubert,Gade, Lutz H.

, p. 14922 - 14928 (2012/02/01)

A new class of chiral tridentate N-donor pincer ligands, bis(oxazolinylmethylidene)isoindolines (boxmi), was synthesized in three steps starting from readily available phthalimides. Their reaction with ethyl (triphenylphosphoranylidene)acetate by means of

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