88097-36-3 Usage
Chemical class
Ester An organic compound formed by the reaction of an acid and an alcohol, characterized by a distinctive fruity smell.
Derivative
1-methyl-2-phenylindole-3-ol A compound derived from the parent molecule, indole, by substituting a hydrogen atom with a methyl group and a phenyl group.
Aromatic compound
The presence of a heterocyclic indole structure A compound containing a benzene ring with a pyrrole fused to it, giving it a distinctive aroma and chemical properties.
Pleasant and sweet floral scent
The chemical is used in perfumes and fragrances due to its appealing odor, which can evoke a sense of freshness and natural beauty.
Potential pharmacological properties
Anti-inflammatory and anti-cancer activities The compound has been studied for its ability to reduce inflammation and inhibit the growth of cancer cells, making it a promising candidate for medicinal applications.
Versatile and valuable chemical
Industrial and therapeutic uses 1H-Indol-3-ol, 1-methyl-2-phenyl-, acetate (ester) has a range of applications in various industries, from the production of scents and flavors to potential use in the development of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 88097-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,9 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88097-36:
(7*8)+(6*8)+(5*0)+(4*9)+(3*7)+(2*3)+(1*6)=173
173 % 10 = 3
So 88097-36-3 is a valid CAS Registry Number.
88097-36-3Relevant academic research and scientific papers
Palladium-catalyzed direct and regioselective C-H bond functionalization/ oxidative acetoxylation of indoles
Choy, Pui Ying,Lau, Chak Po,Kwong, Fuk Yee
supporting information; experimental part, p. 80 - 84 (2011/03/22)
The first general examples of palladium-catalyzed direct and selective oxidative C3-acetoxylation of indoles are presented. The mild reaction conditions (70 °C and with weak base, KOAc) in this indole C-H-acetoxylation are notable.
Oxidation of Indoles with Lead Tetra-acetate and Hydrolysis of 1,2-Disubstituted Indol-3-yl Acetates
Sukari, Mohamed A.,Vernon, John M.
, p. 2219 - 2224 (2007/10/02)
Oxidation of some 1,2-disubstituted indoles with lead tetra-acetate gives the corresponding 3-acetoxy derivatives.Similar oxidation of ethyl indole-2-carboxylate affords an acetoxylated 3,3'-bi-indolyl product; methyl 1-methylindol-3-yl acetate is acetoxylated at the benzylic position of the side-chain.Alkaline hydrolysis of 1,2-disubstituted indol-3-yl acetates is accompanied by autoxidation and rearrangement to give dioxindoles, but hydrolysis of 2-ethoxycarbonyl-1-methylindol-3-yl acetate gives N,N'-dimethyl derivatives of indigo and indirubin.
