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The chemical formula "C8H7(2)H3O2" represents a compound with 8 carbon atoms, 7 hydrogen atoms, and 2 oxygen atoms. The superscript (2) on the hydrogen atom indicates that there are two hydrogen atoms in a specific position or group. C8H7(2)H3O2 is likely an aromatic compound, given the presence of a benzene ring (C6H5) and the substitution of hydrogen atoms with other groups. The presence of two oxygen atoms suggests that the compound may contain functional groups such as a carbonyl group (C=O) or an ether group (R-O-R). The exact structure and properties of the compound would depend on the specific arrangement of these atoms and the nature of the substituents.

7329-56-8

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7329-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7329-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7329-56:
(6*7)+(5*3)+(4*2)+(3*9)+(2*5)+(1*6)=108
108 % 10 = 8
So 7329-56-8 is a valid CAS Registry Number.

7329-56-8Upstream product

7329-56-8Downstream Products

7329-56-8Relevant academic research and scientific papers

Microwave-assisted deuterium exchange: The convenient preparation of isotopically labelled analogues for stable isotope dilution analysis of volatile wine phenols

Crump, Anna M.,Sefton, Mark A.,Wilkinson, Kerry L.

, p. 261 - 263 (2014)

This study reports the convenient, low cost, one-step synthesis of labelled analogues of six volatile phenols, guaiacol, 4-methylguaiacol, 4-ethylguaiacol, 4-ethylphenol, eugenol and vanillin, using microwave-assisted deuterium exchange, for use as intern

Shifted Selectivity in Protonation Enables the Mild Deuteration of Arenes through Catalytic Amounts of Bronsted Acids in Deuterated Methanol

Fischer, Oliver,Hubert, Anja,Heinrich, Markus R.

, p. 11856 - 11866 (2020/10/23)

Taking advantage of the "differentiating effect"of the solvent methanol, deuterations of electron-rich aromatic systems can be carried out under mild acid catalysis and thus under far milder conditions than known so far. The exceptional functional group t

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