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The chemical compound "3-Oxazolidinecarboxylic acid, 2-[(1R)-1-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-4-oxo-7-(phenylmethoxy)heptyl]-4-phenyl-, 1,1-dimethylethyl ester, (2R,4R)-" is a complex organic molecule with a unique structure. It features a 3-oxazolidinecarboxylic acid core, which is a heterocyclic ring containing nitrogen and oxygen. The compound has a chiral center at the 2-position, with a (1R)-configuration, indicating that the hydroxyl group and the attached substituents are arranged in a specific spatial orientation. The molecule also includes a 1,1-dimethylethyl (tert-butyl) ester group, which provides stability and reactivity to the molecule. The presence of a diphenylsilyl ether group and a phenylmethoxy group further contribute to the molecule's complexity, suggesting potential applications in organic synthesis, particularly in the protection of functional groups or as a precursor in the synthesis of more complex molecules.

600143-35-9

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600143-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 600143-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,0,1,4 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 600143-35:
(8*6)+(7*0)+(6*0)+(5*1)+(4*4)+(3*3)+(2*3)+(1*5)=89
89 % 10 = 9
So 600143-35-9 is a valid CAS Registry Number.

600143-35-9Relevant academic research and scientific papers

Enantioselective synthesis of clavepictine analogues and evaluation of their cytotoxic activity

Agami, Claude,Couty, Francois,Evano, Gwilherm,Darro, Francis,Kiss, Robert

, p. 2062 - 2070 (2007/10/03)

Six analogues (labeled 27 to 32) of a cytotoxic alkaloid isolated from the tunicate Clavelina picta were synthesized from an acyl oxazolidine. The absolute stereochemistry of the targeted analogues derived from (R)-phenyl glycinol and the relative stereoc

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