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2-((R)-2-Hydroxy-1-phenyl-ethyl)-hexahydro-isoindole-1,3-dione is a complex organic compound with a molecular formula of C16H19NO3. It is a chiral molecule, with the R-configuration at the 2-hydroxy-1-phenyl-ethyl group. 2-((R)-2-Hydroxy-1-phenyl-ethyl)-hexahydro-isoindole-1,3-dione is characterized by a hexahydro-isoindole-1,3-dione core, which is a cyclic structure with two carbonyl groups and six hydrogen atoms attached to the carbon atoms. The hydroxy-phenyl-ethyl side chain is attached to the 2-position of the isoindole ring, providing a hydroxyl group and a phenyl ring, which can participate in various chemical reactions and interactions. 2-((R)-2-Hydroxy-1-phenyl-ethyl)-hexahydro-isoindole-1,3-dione may have potential applications in pharmaceuticals or as a building block in the synthesis of more complex molecules, but its specific uses and properties would depend on further research and characterization.

86331-30-8

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86331-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86331-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,3 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86331-30:
(7*8)+(6*6)+(5*3)+(4*3)+(3*1)+(2*3)+(1*0)=128
128 % 10 = 8
So 86331-30-8 is a valid CAS Registry Number.

86331-30-8Relevant academic research and scientific papers

AN ASYMMETRIC SYNTHESIS OF BICYCLIC LACTONES AND ITS APPLICATION TO THE ASYMMETRIC SYNTHESIS OF (1R,3S)-CIS-CHRYSANTHEMIC ACID

Mukaiyama, Teruaki,Yamashita, Hiroyuki,Asami, Masatoshi

, p. 385 - 388 (2007/10/02)

Optically active bicyclic lactones are synthesized from imides, derived from (R)-(-)-2-amino-2-phenylethanol and meso-cyclic-1,2-cis-dicarboxylic acids, by successive treatment with sodium bis(2-methoxyethoxy)aluminum hydride and sodium borohydride, followed by acid hydrolysis.This reaction is successfully applied to the asymmetric synthesis of (1R,3S)-cis-chrysanthemic acid.

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