90539-82-5 Usage
Derived from indole
1H-Indol-3-ol, 1-benzoyl-, acetate (ester) is a chemical compound that is derived from indole, a common organic compound found in many plants.
Used in pharmaceutical industry
It is primarily used in the pharmaceutical industry for the synthesis of various drugs and medications.
Ester formation
1H-Indol-3-ol, 1-benzoyl-, acetate (ester) is an ester, which means it is formed from the reaction of an alcohol and a carboxylic acid.
Benzoyl group attachment
The benzoyl group attached to the 1H-indol-3-ol core provides unique chemical properties that make it useful for various pharmaceutical applications.
Potential biological activity
1H-Indol-3-ol, 1-benzoyl-, acetate (ester) may have potential biological activity and could be of interest for further research in drug development.
Importance in pharmaceutical industry
1H-Indol-3-ol, 1-benzoyl-, acetate (ester) is an important chemical with various potential applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 90539-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90539-82:
(7*9)+(6*0)+(5*5)+(4*3)+(3*9)+(2*8)+(1*2)=145
145 % 10 = 5
So 90539-82-5 is a valid CAS Registry Number.
90539-82-5Relevant academic research and scientific papers
Regio- and Stereo-chemical Aspects of Photocycloaddition Between 1-Benzoylindoles and Olefins
Ikeda, Masazumi,Ohno, Kazunori,Mohri, Shin-ichiro,Takahashi, Masami,Tamura, Yasumitsu
, p. 405 - 412 (2007/10/02)
The regio- and stereo-selectivities in the photocycloaddition of a series of 1-benzoylindoles with vinyl acetate and methyl acrylate have been investigated.With some exceptions, the 1-benzoylindoles gave exclusively or predominatly the corresponding 1-acetoxy-3-benzoyl and 3-benzoyl-1-methoxycarbonyl-1,2,2a,7b-tetrahydro-3H-cyclobutindoles as mixtures of stereoisomers.
