147372-91-6 Usage
Derivation
Indole and acetic acid Derived from the combination of a heterocyclic aromatic organic compound (indole) and a simple carboxylic acid (acetic acid).
Usage
Organic synthesis and pharmaceutical research Commonly used in the synthesis of various chemical compounds and in the development of potential drug candidates.
Structural resemblance
Natural indole alkaloids Shares a similar structure with naturally occurring compounds that exhibit various biological activities.
Potential
Building block in heterocyclic compound synthesis Serves as a starting material for the synthesis of other complex heterocyclic compounds with potential pharmaceutical applications.
Biological and pharmacological properties
Limited research The specific properties and effects of 1-phenyl-1H-indol-3-yl acetate have not been extensively studied, and further research is needed to fully understand its potential uses and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 147372-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,3,7 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147372-91:
(8*1)+(7*4)+(6*7)+(5*3)+(4*7)+(3*2)+(2*9)+(1*1)=146
146 % 10 = 6
So 147372-91-6 is a valid CAS Registry Number.
147372-91-6Relevant academic research and scientific papers
Metal-free regioselective C-3 acetoxylation of N-substituted indoles: Crucial impact of nitrogen-substituent
Soni, Vineeta,Patel, Ulhas N.,Punji, Benudhar
, p. 57472 - 57481 (2015/07/20)
A metal-free method for the regioselective C-3 acetoxylation of the N-substituted indoles with PhI(OAc)2 is described under mild reaction conditions. This method tolerates a broad range of functional groups with moderate to good yields. The π-e
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.
