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1-p-tolyl-2-phenyl-1-propanol is an organic compound with the molecular formula C18H20O. It is a colorless to pale yellow liquid with a distinctive aromatic odor. 1-p-tolyl-2-phenyl-1-propanol is characterized by a propanol backbone, with a p-tolyl (4-methylphenyl) group attached to the first carbon and a phenyl group attached to the second carbon. It is synthesized through various chemical reactions, such as the condensation of benzaldehyde with isopropanol in the presence of an acid catalyst. 1-p-tolyl-2-phenyl-1-propanol is used as a fragrance ingredient in the perfume industry, as well as a chemical intermediate in the synthesis of other organic compounds. Due to its complex structure and aromatic nature, it exhibits unique olfactory properties that contribute to its use in creating various scents and flavors.

88980-78-3

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88980-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88980-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,8 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88980-78:
(7*8)+(6*8)+(5*9)+(4*8)+(3*0)+(2*7)+(1*8)=203
203 % 10 = 3
So 88980-78-3 is a valid CAS Registry Number.

88980-78-3Relevant academic research and scientific papers

MECANISME DE L'ADDITION NUCLEOPHILE AU GROUPEMENT CARBONYLE-I. INFLUENCE DE LA NATURE DU SUBSTITUANT POLAIRE SUR LA STEREOCHIMIE ET LA REACTIVITE DANS LES REACTIONS D'ADDITION DE BROMURE DE METHYLMAGNESIUM AUX ARYL-1 PHENYL-2 PROPANONES

Lasperas, M.,Perez-Rubalcaba, A.,Quiroga-Feijoo, M. L.

, p. 3403 - 3408 (1980)

The influence of a m- or p-polar substituent in 1-aryl 2-phenyl propanones, on addition reactions with CH3MgBr in ether at 30 deg C has been investigated.The invariability of asymmetric induction as a function of substituent, and the correlation of rate constant ratios with Hammett ? constants (ρ=0.24, r=0.97), are consistent with a four-centre pericyclic concerted mechanism with concomitant departure of a solvent molecule.

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