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(-)-Abietic acid, also known as abieta-8',11,13-trien-18-oic acid, is a naturally occurring diterpenoid found in the resin of coniferous trees, particularly in the genus Pinus. It is a white crystalline solid with a molecular formula of C20H30O2 and a molecular weight of 302.45 g/mol. This organic compound is an important constituent of rosin, a sticky substance used in various industrial applications such as adhesives, varnishes, and printing inks. (-)-Abietic acid has a unique structure characterized by three conjugated double bonds and a carboxylic acid group, which contribute to its chemical properties and reactivity. It is also used as a precursor in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.

5618-76-8

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5618-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5618-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5618-76:
(6*5)+(5*6)+(4*1)+(3*8)+(2*7)+(1*6)=108
108 % 10 = 8
So 5618-76-8 is a valid CAS Registry Number.

5618-76-8Upstream product

5618-76-8Relevant academic research and scientific papers

A new base mediated method for the cleavage of tert-butyl esters

Paul, Soumendu,Schmidt, Richard R.

, p. 1107 - 1108 (2002)

A new method for the cleavage of tert-butyl esters with NaH in DMF is described.

In depth analysis of chiroptical properties of enones derived from abietic acid

Masnyk, Marek,Butkiewicz, Aleksandra,Górecki, Marcin,Luboradzki, Roman,Paluch, Piotr,Potrzebowski, Marek J.,Frelek, Jadwiga

, p. 3547 - 3561 (2018/04/14)

With the use of inexpensive commercially available abietic acid, a whole series of abietane enones were prepared in high yields. The structures of all the products obtained were determined by comprehensive spectroscopic analysis with particular emphasis on the use of advanced NMR techniques, comparison with previously reported data and, where possible, by single crystal X-ray diffraction. However, in cases where X-ray crystallography was not applicable or compounds tested were unstable, a final stereochemical assignment could be inferred only by electronic circular dichroism (ECD) supported by vibrational circular dichroism to increase credibility. To reveal the relationship between structure and chiroptical properties, we used combined experimental and theoretical analysis of geometries, structural parameters, and chiroptical properties of all enones synthesized. A thorough analysis of their conformational flexibility by examining the effect of solvent and temperature on the ECD spectra was also used to achieve desired objectives. As a result, the impact of substituents adjacent to the enone chromophore on the conformation was determined by demonstrating that even slight changes in the position of hydroxyl and isopropyl groups attached to carbon C13 may substantially affect ECD curves' pattern, leading in some cases to Cotton effects sign reversal.

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