64968-22-5 Usage
Ester derivative
Indole-3-ol and acetic acid 1H-Indol-3-ol, 2-phenyl-, acetate (ester) is an ester formed from the reaction between indole-3-ol (a derivative of indole) and acetic acid.
Usage in perfume and fragrance industry
Pleasant, floral odor 1H-Indol-3-ol, 2-phenyl-, acetate (ester) is commonly used in perfumes and fragrances due to its appealing scent.
Production of pharmaceuticals
Bioactive compound 1H-Indol-3-ol, 2-phenyl-, acetate (ester) is used in the production of pharmaceuticals, as it has potential applications in medicinal chemistry due to its structural similarity to naturally occurring bioactive compounds.
Flavoring agent
Food and beverages 1H-Indol-3-ol, 2-phenyl-, acetate (ester) is also used as a flavoring agent in food and beverages.
Organic synthesis
Structural similarity to bioactive compounds The compound has potential applications in organic synthesis, as its structure is similar to that of naturally occurring bioactive compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 64968-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,6 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64968-22:
(7*6)+(6*4)+(5*9)+(4*6)+(3*8)+(2*2)+(1*2)=165
165 % 10 = 5
So 64968-22-5 is a valid CAS Registry Number.
64968-22-5Relevant academic research and scientific papers
STUDIES ON TERTIARY AMINE OXIDES. LXXII. SOME NUCLEOPHILIC REACTIONS OF 1-HYDROXY-2-PHENYLINDOLE
Nagayoshi, Tsuyoshi,Saeki, Seitaro,Hamana, Masatomo
, p. 1920 - 1926 (2007/10/02)
1-Hydroxy-2-phenylindole (1) reacts with tosyl chloride and p-nitrobenzenesulfonyl chloride in DMF-pyridine to give the corresponding 2-phenyl-3-sulfonyloxyindole (2 and 4).Benzoyl chloride is less reactive, and 1-benzoyloxy-2-phenylindole (5) or 3-benzoyloxy-2-phenylindole (6) is formed, depending upon the reaction conditions. 3-Acetoxy-2-phenylindole (7) is also obtained by refluxing 1 with acetic anhydride or with acetyl chloride in DMF-pyridine.Treatment of 1 with tosyl chloride and then with 1-morpholinocyclohexene (9), ethyl acetoacetate (17) and ethyl cyanoacetate (20) in DMF-pyridine at room temperature affords 3-(2-oxocyclohexyl)-2-phenylindole (10), ethyl α-(2-phenyl-3-indolyl)acetoacetate (18) and ethyl α-(2-phenyl-3-indolyl)cyanoacetate (21) in 23.2, 41 and 61percent yields, respectively.Keywords: enehydroxylamine system; 1-acyloxy-2-phenylindole; 3-acyloxy-2-phenylindole; 1-morpholinocyclohexene; 3-(2-oxocyclohexyl)-2-phenylindole; ethyl α-(2-phenyl-3-indolyl)acetoacetate; ethyl α-(2-phenyl-3-indolyl)cyanoacetate
