17152-81-7 Usage
Uses
Used in Cosmetic and Personal Care Industry:
Phenol, 4-(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)is used as a fragrance and flavor ingredient for its aromatic and minty scent in various cosmetic and personal care products such as perfumes, soaps, and lotions. Its pleasant odor enhances the sensory experience of these products, making them more appealing to consumers.
Used in Antimicrobial Formulations:
Due to its antimicrobial properties, Phenol, 4-(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)is utilized in certain topical antiseptic formulations. It helps to prevent the growth of harmful microorganisms on the skin, promoting better hygiene and reducing the risk of infections.
Used in Pharmaceutical and Medical Industries:
Phenol, 4-(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)may have potential applications in the pharmaceutical and medical industries. Its unique chemical structure and properties could be harnessed for the development of new drugs or medical treatments, although further research is needed to explore these possibilities.
Check Digit Verification of cas no
The CAS Registry Mumber 17152-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17152-81:
(7*1)+(6*7)+(5*1)+(4*5)+(3*2)+(2*8)+(1*1)=97
97 % 10 = 7
So 17152-81-7 is a valid CAS Registry Number.
17152-81-7Relevant academic research and scientific papers
Alkylation of phenol by β-pinene in the presence of aluminum phenolate
Chukicheva,Shumova,Kuchin
experimental part, p. 43 - 46 (2012/07/17)
The alkylation of phenol by β-pinene using Al(OPh)3 as a catalyst was studied. It was found that the composition of the products depended on the ratio of starting materials. The principal products were chromane-type ethers with an equimolar ratio of starting materials and an excess of phenol. ortho-Alkylated phenol and an ether with a terpene substituent of bornyl structure were formed with a two-fold excess of β-pinene.
Tandem molecular rearrangement in the alkylation of phenol with camphene
Chukicheva,Spirikhin,Kuchin
, p. 62 - 66 (2008/12/21)
The alkylation of phenol with camphene in the presence of boron trifluoride in glacial acetic acid was accompanied by tandem molecular rearrangement with formation of a mixture of ortho- and para-substituted phenols having 1,7,7-trimethylbicyclo[2.2.1]hept-exo-2-yl and 5,5,6-trimethylbicyclo[2.2.1] hept-exo-2-yl substituents. The same products were obtained by rearrangement of 1,7,7-trimethylbicyclo[2.2.1]hept-exo-2-yloxybenzene under analogous conditions. Similar reactions performed in the presence of aluminum phenoxide as catalyst resulted in predominant formation of the corresponding ortho-substituted phenols.
