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C9H12O2 is an organic compound with a molecular formula indicating it contains 9 carbon atoms, 12 hydrogen atoms, and 2 oxygen atoms. C9H12O2 could represent a variety of organic molecules, such as certain phenolic compounds or derivatives of benzoic acid. Without additional information, it's challenging to specify the exact structure or properties. However, compounds with this formula often exhibit characteristics typical of aromatic or phenolic structures, which may include reactivity with bases due to the presence of acidic hydrogens and potential for forming esters or other derivatives due to the oxygen atoms.

7287-92-5

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7287-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7287-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,8 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7287-92:
(6*7)+(5*2)+(4*8)+(3*7)+(2*9)+(1*2)=125
125 % 10 = 5
So 7287-92-5 is a valid CAS Registry Number.

7287-92-5Upstream product

7287-92-5Downstream Products

7287-92-5Relevant academic research and scientific papers

Selective catalytic aerobic oxidation of substituted ethylbenzenes under mild conditions

Melone, Lucio,Prosperini, Simona,Gambarotti, Cristian,Pastori, Nadia,Recupero, Francesco,Punta, Carlo

, p. 155 - 160 (2012)

Ethylbenzene is oxidized to the corresponding hydroperoxide (PEHP) with high selectivity, under mild conditions, by means of a metal-free catalytic system consisting of an aldehyde and N-hydroxyphthalimide (NHPI). The process occurs via a free radical mechanism by in situ generation of the phthalimido-N-oxyl (PINO) radical. The protocol is applied with success on a wide range of substituted ethylbenzenes (ETBs). The competitive experiments carried out on few couples of ETBs revealed a marked polar effect, this proving the key role that PINO plays as real hydrogen abstracting species, at least at low conversion. At higher conversion, the formation of highly reactive OH radicals from PEHP reduces the differences in the reactivity of selected couples of ETBs. The study of the reaction mechanism, including the investigation on aldehyde and catalyst percentage amounts, and temperature and concentration effects, allows to achieve the final PEHPs products with good yields.

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