33781-37-2 Usage
Uses
Used in Fragrance and Flavor Industry:
2,3-Dihydro-5-methyl-1H-inden-1-ol is used as a key ingredient in the fragrance and flavor industry for its distinct floral odor, enhancing the sensory experience of various products such as perfumes, colognes, and food flavorings.
Used in Pharmaceutical Applications:
In the pharmaceutical sector, 2,3-dihydro-5-methyl-1H-inden-1-ol is utilized as a potential therapeutic agent due to its antioxidant and anti-inflammatory properties. These characteristics make it a candidate for the development of treatments targeting a range of conditions that involve oxidative stress and inflammation.
Used in Cosmetic Applications:
Within the cosmetic industry, 2,3-dihydro-5-methyl-1H-inden-1-ol is employed as an active ingredient for its beneficial effects on skin health. Its antioxidant and anti-inflammatory properties contribute to the development of skincare products that aim to protect and rejuvenate the skin.
Used in Organic and Medicinal Chemistry Research:
2,3-Dihydro-5-methyl-1H-inden-1-ol is also used as a subject of study in organic and medicinal chemistry. Its unique structure and properties make it an important molecule for understanding chemical reactions and exploring its potential in the synthesis of new compounds with therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 33781-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,8 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33781-37:
(7*3)+(6*3)+(5*7)+(4*8)+(3*1)+(2*3)+(1*7)=122
122 % 10 = 2
So 33781-37-2 is a valid CAS Registry Number.
33781-37-2Relevant academic research and scientific papers
Substituent Effect Behavior in the Antiaromatic Inden-1-yl Cation System
Friedrich, Edwin C.,Tam, Teresa M.
, p. 315 - 319 (2007/10/02)
Studies of the rate-accelerating effects in solvolysis produced by 5-methyl and 5-methoxy substituents on the benzene ring and a 3-methyl substituent on the double bond of the inden-1-yl 3,5-dinitrobenzolate system have been carried out.In both 80percent aqueous acetone and in 2,2,2-trifluoroethanol, the rate accelerations observed in the inden-1-yl system were approximately the same as those found in model cyclopenten-3-yl and indan-1-yl systems.From these results, it is concluded that delocalization of charge into both the benzene ring and double bond of the 8?-electron inden-1-yl carbocation is taking place and is apparently undiminished by antiaromatic effects.
