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β-2,3-diphenyl-4,4-dimethylpentan-3-ol is a complex organic compound with the molecular formula C19H24O. It is a secondary alcohol, characterized by the presence of a hydroxyl group (-OH) attached to a carbon atom in the third position of a pentane chain. The molecule features two phenyl rings (C6H5) attached to the second and third carbon atoms of the pentane chain, and two methyl groups (-CH3) attached to the fourth carbon atom. This chemical structure endows the compound with unique properties, such as its potential use in the synthesis of pharmaceuticals and other organic compounds. Due to its specific arrangement of functional groups and aromatic rings, β-2,3-diphenyl-4,4-dimethylpentan-3-ol may exhibit distinct chemical reactivity and physical characteristics compared to other related compounds.

70303-20-7

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70303-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70303-20-7 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, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70303-20:
(7*7)+(6*0)+(5*3)+(4*0)+(3*3)+(2*2)+(1*0)=77
77 % 10 = 7
So 70303-20-7 is a valid CAS Registry Number.

70303-20-7Downstream Products

70303-20-7Relevant 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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