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β-2,3-diphenyl-4-methylpentan-3-ol is a complex organic compound with the molecular formula C17H20O. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is known for its unique structure that features two phenyl rings attached to a central pentane chain, with a methyl group at the fourth carbon and a hydroxyl group at the third carbon. β-2,3-diphenyl-4-methylpentan-3-ol is of interest in the field of organic chemistry, particularly in the synthesis of certain pharmaceuticals and as a precursor in the production of various chemical compounds. Its specific applications and properties can vary depending on the context in which it is used, and further research may reveal additional uses or characteristics.

70303-14-9

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70303-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70303-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,0 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70303-14:
(7*7)+(6*0)+(5*3)+(4*0)+(3*3)+(2*1)+(1*4)=79
79 % 10 = 9
So 70303-14-9 is a valid CAS Registry Number.

70303-14-9Downstream Products

70303-14-9Relevant academic research and scientific papers

Stereoselectivity in the Condensation Reactions of 1-Phenylethyl Alkyl and Phenyl Ketones with Organometallic Reagents

Alvarez-Ibarra, Carlos,Arjona, Odon,Perez-Ossorio, Rafael,Perez-Rubalcaba, Alfredo,Quiroga, Maria L.,Santesmases, Maria J.

, p. 1645 - 1648 (2007/10/02)

Stereochemical results of the condensation reactions of a series of ketones, PhCHMeCOR (R= Me, Et, Pri, But, Ph), with various organomagnesium and organolithium derivatives in ethers as solvents are reported.Results are accounted for on the basis of competition between two transition states which may adopt either Karabatsos- or Felkin-type conformations according to the nature of R, the reagent nucleophilicity, and the polarity of solvent.Polar and steric analysis of this reaction allows highly stereoselective syntheses of diastereoisomeric α-phenylalkanols to be devised.

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