175136-13-7 Usage
Description
1-(4-Hydroxy-7-methyl-indan-5-yl)-ethanone is a chemical compound with the molecular formula C13H14O2. It is a ketone compound that contains a unique indan ring structure and an attached hydroxy and methyl group. 1-(4-HYDROXY-7-METHYL-INDAN-5-YL)-ETHANONE is commonly used in organic chemical synthesis and pharmaceutical research.
Used in Pharmaceutical Research:
1-(4-Hydroxy-7-methyl-indan-5-yl)-ethanone is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Organic Chemical Synthesis:
1-(4-Hydroxy-7-methyl-indan-5-yl)-ethanone is used as a versatile building block in the synthesis of complex organic molecules. Its reactivity and functional groups allow for a wide range of chemical reactions, making it a valuable component in the creation of novel organic compounds.
Further Research:
1-(4-Hydroxy-7-methyl-indan-5-yl)-ethanone warrants further research to explore its potential biological activities and pharmacological effects. Understanding its interactions with biological systems could lead to the discovery of new applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 175136-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175136-13:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*6)+(2*1)+(1*3)=127
127 % 10 = 7
So 175136-13-7 is a valid CAS Registry Number.
175136-13-7Relevant articles and documents
Titanium(IV) chloride-mediated ortho-acylation of phenols and naphthols
Bensari, Ahlem,Zaveri, Nurulain T.
, p. 267 - 271 (2003)
The use of titanium(IV) chloride as a Lewis acid for direct ortho-acylation of phenols and naphthols proves to be a convenient, more general and direct route to various hydroxyaryl ketones. The route is regioselective, leading to ortho C-acylated products in satisfactory to high yields in most cases.