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Hydroxy-cyclopentyl-diphenyl-methan, also known as hydroxy-cyclopentyl-diphenylmethane, is a complex organic compound with the molecular formula C18H20O. It is characterized by a cyclopentyl ring, which is a five-membered carbon ring, attached to a diphenylmethane group, consisting of two phenyl rings (C6H5) connected to a central methyl group (CH3). The hydroxyl group (-OH) is present, indicating the presence of an alcohol functional group. Hydroxy-cyclopentyl-diphenyl-methan is known for its potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and other organic compounds. Its unique structure allows for a range of chemical reactions and interactions, making it a valuable component in the development of new materials and medicines.

4479-29-2

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4479-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4479-29-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,7 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4479-29:
(6*4)+(5*4)+(4*7)+(3*9)+(2*2)+(1*9)=112
112 % 10 = 2
So 4479-29-2 is a valid CAS Registry Number.

4479-29-2Relevant academic research and scientific papers

NBS-promoted rearrangement of 1,1-diarylmethylenecyclopentane

Chang, Meng-Yang,Lin, Chung-Han

scheme or table, p. 853 - 856 (2012/02/05)

The 1-aroyl-1-aryl-2-bromocyclopentanes 3a, 3b, 3c and 3d (Ar = C 6H5, 2-FC6H4, 3-FC6H 4, 4-FC6H4) were prepared from N-bromosuccinimide (NBS)-promoted rearrangement o

Hydrocarbon activation. Synthesis of β-cycloalkyl (Di)nitriles through photosensitized conjugate radical addition

Cardarelli,Fagnoni,Mella,Albini

, p. 7320 - 7327 (2007/10/03)

Photoinduced hydrogen abstraction from aliphatic cyclic hydrocarbons (C5 to C7, C12, as well as adamantane) by triplet aromatic ketones in the presence of α,β-unsaturated (di)nitriles offers a straightforward entry to the corresponding alkylated (di)nitriles via the alkyl radicals. Yields are moderate to good depending on the olefins structure (substitution in β slows down the addition to mononitriles, but with α,α-dinitriles electronic activation allows efficient alkylation also of β,β-disubstituted substrates). A tandem alkylation - cyclization process has been obtained with (1-methylpent-4-enylidene)malononitrile.

Adjusting the top end of the alkyl radical kinetic scale. Laser flash photolysis calibrations of fast radical clocks and rate constants for reactions of benzeneselenol

Newcomb,Choi,Horner

, p. 1225 - 1231 (2007/10/03)

Rate constants for 5-exo cyclizations of the 6,6-diphenyl-5-hexenyl radical (1a), the 1-methyl-6,6-diphenyl-5-hexenyl radical (1b), and the 1,1- dimethyl-6,6-diphenyl-5-hexenyl radical (1c) were measured by laser flash photolysis methods, and Arrhenius parameters for these cyclizations were determined. Relative rate constants for cyclizations of radicals 1 and reactions with benzeneselenol were determined by indirect kinetic methods, and the relative Arrhenius parameters for the competing reactions were combined with the parameters for the cyclization reactions to give absolute Arrhenius parameters for the PhSeH reactions. At 20 °C, PhSeH reacts with the 1°, 2°, and 3°radicals 1 with nearly the same rate constants, (1.2 ± 0.1) x 109 M-1 s-1. Absolute Arrhenius parameters for reactions of PhSH and t-BuSH with the primary alkyl radical 1a were calculated using literature values for the competition between cyclization of 1a and reactions with the appropriate thiol and the absolute values for cyclization of 1a determined in this work. The results suggest that rate constants for reactions of primary alkyl radicals with t-BuSH are about 20% smaller than those previously reported. In the case of PhSH, the results are in good agreement with one previously reported set of rate constants but about 35% smaller than another set of rate constants that was subsequently incorporated into fast alkyl radical kinetics. The rate constants for alkyl radical reactions calibrated by competition against reaction with PhSeH and PhSH apparently are 30-40% smaller than those previously reported, and the derived rate constants for the fast radical reactions should be adjusted. An especially noteworthy example is ring opening of the cyclopropylcarbinyl radical, the Arrhenius function for which was determined in part from PhSH trapping results. Using the adjusted rate constants for PhSH and recalculating the Arrhenius parameters for the cyclopropylcarbinyl radical ring opening gives log(k/s- 1) = (13.045 ± 0.10) (6.99 ± 0.09)/θ (kcal/mol, errors at 2σ); the rate constant at 20 °C of 6.7 x 107 s-1 is about 13% smaller than that previously calculated.

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