55255-94-2 Usage
Chemical class
Naphthalenols 1,2,3,4-Tetrahydro-1,4-methanonaphthalen-9-ol belongs to a class of organic compounds known as naphthalenols, which are characterized by a naphthalene ring with one or more hydroxyl groups attached.
Physical state
Colorless liquid Tetrahydrodiosphenol is a colorless liquid at room temperature, making it easy to handle and mix with other ingredients in various applications.
Odor
Strong, sweet floral 1,2,3,4-Tetrahydro-1,4-methanonaphthalen-9-ol has a strong, sweet, and floral odor, which makes it a popular choice for use in the fragrance industry.
Uses
Fragrance ingredient Tetrahydrodiosphenol is commonly used as a fragrance ingredient in perfumes and personal care products due to its pleasant and distinctive scent.
Synthesis
Organic compound synthesis 1,2,3,4-Tetrahydro-1,4-methanonaphthalen-9-ol is also used in the synthesis of other organic compounds, making it a versatile building block in the chemical industry.
Potential applications
Pharmaceutical and agrochemical industries Tetrahydrodiosphenol has potential applications in the pharmaceutical and agrochemical industries, although specific uses have not been detailed in the provided material.
Importance in scents and flavors
Aromatic properties The unique aromatic properties of tetrahydrodiosphenol make it a valuable component in the creation of scents and flavors for various products.
Structural features
Tetrahydro-1,4-methanonaphthalene core The compound has a tetrahydro-1,4-methanonaphthalene core, which is a partially hydrogenated naphthalene ring fused to a cyclopropane ring.
Functional group
Hydroxyl group Tetrahydrodiosphenol contains a hydroxyl (-OH) functional group, which is responsible for its naphthalenol classification and contributes to its unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 55255-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,5 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55255-94:
(7*5)+(6*5)+(5*2)+(4*5)+(3*5)+(2*9)+(1*4)=132
132 % 10 = 2
So 55255-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O/c12-11-9-5-6-10(11)8-4-2-1-3-7(8)9/h1-4,9-12H,5-6H2
55255-94-2Relevant academic research and scientific papers
Okada, Keiji,Tomita, Seiji,Oda, Masaji
, p. 2645 - 2648 (1986)
Electronic control of the anti/syn stereoselectivity in metal hydride reductions of 7-benzonorbornenones 2a-d is proposed.
LIGHT-MEDIATED TRANSFORMATIONS OF OLEFINS INTO ALCOHOLS: REACTIONS OF HYDROXYL RADICALS WITH CYCLOALKENES
Sonawane, H. R.,Nanjundiah, B. S.,Kelkar, R. G.
, p. 6673 - 6682 (2007/10/02)
Reactions of hydroxyl radicals, generated by photodecomposition of hydrogen peroxide in acetonitrile, with a wide variety of cycloalkenes have been examined.The results show that the major reaction is the addition of hydroxyl radicals to the less substituted end of the double bond, furnishing the secondary alcohols.The reactivity pattern and the observed regio- and stereoselectivity clearly reveal that the steric parameters associated with the substrates play a dominant role in directing the addition reactions.More importantly, this study led to the development of a new methodology for the facile conversions of olefins essentially into secondary alcohols, and includes a few examples which demonstrate the potential of the method.
