5402-37-9 Usage
Description
4-(1-Indanyl)phenol, with the molecular formula C19H16O, is an organic compound that falls under the category of phenols. These are aromatic compounds characterized by the presence of a hydroxyl group attached to a benzene ring. In the case of 4-(1-Indanyl)phenol, the hydroxyl group is bonded to the 4th carbon atom of the benzene ring. 4-(1-INDANYL)PHENOL's name also reflects the indane ring system that is fused to the benzene ring, giving it a distinctive structure. This structure, along with the antioxidant properties commonly associated with phenols, positions 4-(1-Indanyl)phenol as a compound of interest in pharmaceuticals, organic chemistry, and material science research.
Uses
Used in Pharmaceutical Industry:
4-(1-Indanyl)phenol is used as a starting material for the synthesis of various drugs and pharmaceutical products due to its phenolic nature and potential antioxidant properties. Its unique structure also makes it a valuable compound for the development of new medications.
Used in Organic Chemistry Research:
The distinctive fused ring structure of 4-(1-Indanyl)phenol makes it a subject of interest for research in organic chemistry. Its properties and potential reactions can provide insights into the development of new chemical compounds and processes.
Used in Material Science:
4-(1-Indanyl)phenol's unique structure and properties also make it a compound of interest for research in material science. Its potential applications in the development of new materials or the enhancement of existing ones are areas of exploration.
Check Digit Verification of cas no
The CAS Registry Mumber 5402-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5402-37:
(6*5)+(5*4)+(4*0)+(3*2)+(2*3)+(1*7)=69
69 % 10 = 9
So 5402-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O/c16-13-8-5-12(6-9-13)15-10-7-11-3-1-2-4-14(11)15/h1-6,8-9,15-16H,7,10H2
5402-37-9Relevant articles and documents
Gold-Catalyzed Friedel–Crafts-Like Reaction of Benzylic Alcohols to Afford 1,1-Diarylalkanes
Oakley, James V.,Stanley, Tyler J.,Jesse, Kate A.,Melanese, Amanda K.,Alvarez, Araceli A.,Prince, Aloha L.,Cain, Stephanie E.,Wenzel, Anna G.,Iafe, Robert G.
supporting information, p. 7063 - 7066 (2019/11/14)
A gold-catalyzed, Friedel–Crafts-like benzylation of unactivated benzylic alcohols to form 1,1-diarylalkanes has been developed. The operationally convenient method uses only 1.3 equivalents of the electron-rich arene, employs readily available starting m
A Systematic Study of Benzyl Cation Initiated Cyclization Reactions
Angle, Steven R.,Louie, Michael S.
, p. 2853 - 2866 (2007/10/02)
A systematic investigation of benzyl cation inititiated cyclization reactions to form six-membered carbocycles is presented.The generation of benzyl cations from benzylic bromides, ethers, and alcohols followed by intramolecular capture provided good yields of cyclized products by use of several different cyclization terminators (e.g., phenyl, alkene, β-keto ester).A study on the effect of changing the electronic nature of substituents para to the benzyl cation showed that even electron-withdrawing substituents such as quaternary ammonium afford high yields of cyclization products.The formation of five- and seven-membered carbocycles was briefly investigated and found to be less general than the formation of the corresponding six-membered carbocycles.
