117788-50-8 Usage
Explanation
Aromatic compounds are characterized by the presence of a benzene ring, which is a six-membered ring with alternating double bonds and delocalized electrons.
3. Benzene ring with two hydroxyl groups
Explanation
The compound has a benzene ring (C6H5) with two hydroxyl (OH) groups attached to it, making it a diol.
4. Heptyl chain attached to one hydroxyl group
Explanation
A heptyl chain, which is a seven-carbon alkyl chain (C7H15), is attached to one of the hydroxyl groups in the molecule.
Explanation
Phenols are a class of chemical compounds consisting of a hydroxyl group (OH) bonded directly to an aromatic hydrocarbon group, in this case, a benzene ring.
Explanation
The common name for 1,2-Benzenediol,3-heptyl-(9CI) is heptylresorcinol, which is derived from its chemical structure and properties.
7. Industrial and commercial applications
Explanation
Heptylresorcinol is used in various industries, including skincare, personal care products, and food packaging materials.
8. Skincare ingredient
Explanation
Heptylresorcinol is used in the skincare industry for its potential antimicrobial, antifungal, and anti-inflammatory properties.
9. Preservative in personal care products
Explanation
Due to its antimicrobial properties, heptylresorcinol is used as a preservative in personal care products to prevent the growth of microorganisms.
10. Antioxidant in food packaging materials
Explanation
Heptylresorcinol acts as an antioxidant in food packaging materials, helping to prevent the oxidation of fats and oils, which can lead to spoilage and rancidity.
11. Potential antimicrobial properties
Explanation
Heptylresorcinol has been studied for its ability to inhibit the growth of microorganisms, making it a potential candidate for use in antimicrobial applications.
12. Potential antifungal properties
Explanation
The compound has been investigated for its ability to inhibit the growth of fungi, which could be useful in various industries, including agriculture and healthcare.
13. Potential anti-inflammatory properties
Explanation
Heptylresorcinol has been studied for its potential to reduce inflammation, which could be beneficial in the development of anti-inflammatory drugs and treatments.
Family
Phenols
Check Digit Verification of cas no
The CAS Registry Mumber 117788-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,8 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117788-50:
(8*1)+(7*1)+(6*7)+(5*7)+(4*8)+(3*8)+(2*5)+(1*0)=158
158 % 10 = 8
So 117788-50-8 is a valid CAS Registry Number.
117788-50-8Relevant articles and documents
Scope and limitations of lithium-ethylenediamine-THF-mediated cleavage at the α-position of aromatics: Deprotection of aryl methyl ethers and benzyl ethers under mild conditions
Shindo, Takeyuki,Fukuyama, Yasuaki,Sugai, Takeshi
, p. 692 - 700 (2007/10/03)
The scope and limitation of lithium-ethylenediamine-THF-mediated reductive bond cleavage at the α-position of aromatics were examined. Very mild conditions such as lithium metal (5 equiv) and ethylenediamine (7 equiv) in oxygen-free THF were quite effective for the demethylation of aromatic ethers even at as low as -10°C. Allyl benzyl ethers were also deprotected under these conditions with very little change of the allylic alcohol moiety. Through this study, 2,6-dimethylbenzyl (m-xylylmethyl, MXM) group was developed as an alternative of benzyl group, which is readily cleavable under the above mentioned reductive conditions.
A quantitative structure-activity relationship for antitumor activity of long-chain phenols from Ginkgo biloba L.
Itokawa,Totsuka,Nakahara,Maezuru,Takeya,Kondo,Inamatsu,Morita
, p. 1619 - 1621 (2007/10/02)
-
