4197-84-6 Usage
Description
2-cyclooctylbenzene-1,4-diol, also known as troloxide, is a chemical compound with the molecular formula C14H20O2. It is a dihydroxybenzene derivative that contains a cyclooctyl group. This chemical is commonly used as an antioxidant and free radical scavenger in various applications, including in the pharmaceutical and food industries. It is also used in the synthesis of various organic compounds due to its versatile reactivity. Troloxide has been investigated for its potential therapeutic properties, including its ability to protect cells from oxidative stress and inflammation. Overall, 2-cyclooctylbenzene-1,4-diol is an important chemical with various industrial and medicinal uses.
Uses
Used in Pharmaceutical Industry:
2-cyclooctylbenzene-1,4-diol is used as an antioxidant and free radical scavenger for protecting cells from oxidative stress and inflammation.
Used in Food Industry:
2-cyclooctylbenzene-1,4-diol is used as an antioxidant to extend the shelf life of food products and maintain their quality.
Used in Organic Synthesis:
2-cyclooctylbenzene-1,4-diol is used as a versatile reagent in the synthesis of various organic compounds.
Used in Antioxidant Applications:
2-cyclooctylbenzene-1,4-diol is used as an antioxidant to protect cells from oxidative stress and inflammation, which can help in the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 4197-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,9 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4197-84:
(6*4)+(5*1)+(4*9)+(3*7)+(2*8)+(1*4)=106
106 % 10 = 6
So 4197-84-6 is a valid CAS Registry Number.
4197-84-6Relevant articles and documents
Synthesis of 2-substituted hydroquinone derivatives from 1,4-benzoquinone and allyl ethers
Kaurich, Kevin J.,Deck, Paul A.
, p. 2191 - 2196 (2018/03/28)
B-Alkylpinacolboranes, derived from rhodium-catalyzed hydroboration of allyl ethers with pinacolborane, react with 1,4-benzoquinone under acidic, oxidizing conditions, to afford, after subsequent hydrogenation, 2-substituted hydroquinones in isolated, pur