21370-71-8 Usage
Description
TRANS-1-DECALONE is a chemical compound derived from essential oils isolated from Citrus aurantium. It is known for its antimicrobial and antioxidant properties, making it a valuable component in various applications.
Uses
Used in Antimicrobial Applications:
TRANS-1-DECALONE is used as an antimicrobial agent for its ability to inhibit the growth of harmful microorganisms. This property makes it suitable for use in the pharmaceutical, food, and cosmetic industries to ensure the safety and longevity of products.
Used in Antioxidant Applications:
TRANS-1-DECALONE is used as an antioxidant to prevent the oxidation of other compounds, which can lead to spoilage or degradation. Its antioxidant properties are beneficial in the food and cosmetic industries, where it can help maintain the freshness and quality of products.
Used in Research and Development:
TRANS-1-DECALONE is used as a subject for studying its proton resonance spectra using Nuclear Magnetic Resonance (NMR) techniques. This application is particularly relevant in the scientific and academic fields, where understanding the structure and properties of chemical compounds is crucial for further research and development.
Used in the Pharmaceutical Industry:
TRANS-1-DECALONE is used as an active ingredient in the development of new drugs and treatments, thanks to its antimicrobial and antioxidant properties. Its potential applications in this industry include the creation of novel antibiotics, antifungal agents, and other therapeutic compounds.
Used in the Food Industry:
TRANS-1-DECALONE is used as a preservative and additive in the food industry to extend the shelf life of products and maintain their quality. Its antimicrobial properties help prevent spoilage caused by bacteria, yeast, and mold, while its antioxidant properties protect against the negative effects of oxidation.
Used in the Cosmetic Industry:
TRANS-1-DECALONE is used as an ingredient in cosmetics for its antimicrobial and antioxidant properties. It can help maintain the freshness and effectiveness of cosmetic products, as well as provide additional benefits such as skin protection and nourishment.
Check Digit Verification of cas no
The CAS Registry Mumber 21370-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,7 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21370-71:
(7*2)+(6*1)+(5*3)+(4*7)+(3*0)+(2*7)+(1*1)=78
78 % 10 = 8
So 21370-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h8-9H,1-7H2
21370-71-8Relevant articles and documents
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Gutsche,Peter
, (1963)
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Chemoselective Oxidation of Equatorial Alcohols with N-Ligated λ3-Iodanes
Mikhael, Myriam,Adler, Sophia A.,Wengryniuk, Sarah E.
supporting information, p. 5889 - 5893 (2019/08/26)
The site-selective and chemoselective functionalization of alcohols in complex polyols remains a formidable synthetic challenge. Whereas significant advancements have been made in selective derivatization at the oxygen center, chemoselective oxidation to the corresponding carbonyls is less developed. In cyclic systems, whereas the selective oxidation of axial alcohols is well known, a complementary equatorial selective process has not yet been reported. Herein we report the utility of nitrogen-ligated (bis)cationic λ3-iodanes (N-HVIs) for alcohol oxidation and their unprecedented levels of selectivity for the oxidation of equatorial over axial alcohols. The conditions are mild, and the simple pyridine-ligated reagent (Py-HVI) is readily synthesized from commercial PhI(OAc)2 and can be either isolated or generated in situ. Conformational selectivity is demonstrated in both flexible 1,2-substituted cyclohexanols and rigid polyol scaffolds, providing chemists with a novel tool for chemoselective oxidation.
Alkane oxidation catalysed by a self-folded multi-iron complex
Mettry, Magi,Moehlig, Melissa Padilla,Gill, Adam D.,Hooley, Richard J.
, p. 120 - 128 (2016/11/09)
A preorganised ligand scaffold is capable of coordinating multiple Fe(II) centres to form an electrophilic CH oxidation catalyst. This catalyst oxidises unactivated hydrocarbons including simple, linear alkanes under mild conditions in good yields with selectivity for the oxidation of secondary CH bonds. Control complexes containing a single metal centre are incapable of oxidising unstrained linear hydrocarbons, indicating that participation of multiple centres aids the CH oxidation of challenging substrates.
An iron catalyst for oxidation of alkyl C-H bonds showing enhanced selectivity for methylenic sites
Prat, Irene,Gomez, Laura,Canta, Merce,Ribas, Xavi,Costas, Miquel
supporting information, p. 1908 - 1913 (2013/03/14)
Many are called but few are chosen: A nonheme iron complex catalyzes the oxidation of alkyl C-H bonds by using H2O2 as the oxidant, showing an enhanced selectivity for secondary over tertiary C-H bonds (see scheme). Copyright