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1-Phenyl-heptadecan-1-ol is an organic compound with the molecular formula C23H38O. It is a long-chain alcohol with a phenyl group attached to the first carbon atom of a heptadecanol backbone. 1-phenyl-heptadecan-1-ol is characterized by its unique structure, which combines the properties of a phenyl ring with a long aliphatic chain. It is a colorless to pale yellow liquid with a specific aroma and is insoluble in water but soluble in organic solvents. 1-Phenyl-heptadecan-1-ol has potential applications in the fragrance industry due to its scent, and it may also be used as a chemical intermediate in the synthesis of various pharmaceuticals and specialty chemicals.

1851-96-3

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1851-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1851-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1851-96:
(6*1)+(5*8)+(4*5)+(3*1)+(2*9)+(1*6)=93
93 % 10 = 3
So 1851-96-3 is a valid CAS Registry Number.

1851-96-3Relevant academic research and scientific papers

Rates and Alkyl Group Size in Solvolysis of Alkyl Derivatives

Orlovic, Mirko,Kronja, Olga,Humski, Kresimir,Borcic, Stanko,Polla, Eugenio

, p. 3253 - 3256 (1986)

The logarithm of solvolysis rate constants in 80percent aqueous ethanol of 1,1-dimethyl-1-alkyl chlorides 1 and 1-phenyl-1-alkyl chlorides 2 decrease monotonically with increasing number of carbon atoms in the alkyl group.The first member of both series deviates from the corresponding correlation lines which have the some slope.In contrast, solvolysis rates in 80percent aqueous ethanol of 1-methyl-1-alkyl tosylates 3 do not depend upon the size of the alkyl group.The results are rationalized in terms of a mechanism that is very similar in reactions of series 1 and 2 but different from that of series 3.

Reductive Transformations, 19. Electron-Transfer-Induced Dimerization of β-Alkylstyrenes and the Structures of Resulting 1,4-Dilithiobutanes

Schade, Peter,Schaefer, Thomas,Muellen, Klaus,Bender, Dietmar,Knoll, Konrad,Bronstert, Klaus

, p. 2833 - 2842 (2007/10/02)

Upon reaction with lithium β-alkylstyrenes undergo dimerization of the resulting radical anions with the formation of 2,3-dialkyl-1,4-dilithio-1,4-diphenyl butanes 1-8.The structure and dynamic behavior of these dilithium organyls are investigated by cryoscopic measurements and 1H-, 13C-, and 6Li-NMR spectroscopy at different temperatures.The butane chain adopts a cisoid conformation; the two benzyl subunits chelate one lithium cation while the other is solvent-separated from the hydrocarbon frame.Depending on the size of the alkyl substitutents and the reaction temperature, the dimerization of the radical anions with the formation of two stereogenic centers can proceed diastereoselectively.Key Words: Lithium organyls/ 1,4-Dilithiobutanes, conformation of ,ion paris of, aggregation of

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