90539-84-7 Usage
Derivative of indole
Indole is a heterocyclic compound 1H-Indole-2-carbonitrile, 1-benzoylis derived from indole, which is a naturally occurring compound found in many natural products and pharmaceuticals.
Building block in pharmaceutical synthesis
Used in the synthesis of various pharmaceutical compounds This compound serves as a starting material or building block for creating a variety of pharmaceutical products.
Intermediate in agrochemical and dye manufacturing
Employed as an intermediate in the manufacturing process 1H-Indole-2-carbonitrile, 1-benzoylis used as an intermediate in the production of agrochemicals and dyes, aiding in the formation of the final products.
Versatile reactivity
Has potential applications in the pharmaceutical and chemical industries Due to its ability to react with a wide range of other chemicals, 1H-Indole-2-carbonitrile, 1-benzoylis a valuable compound in both pharmaceutical and chemical industries.
Wide range of synthetic uses
Utilized in various chemical reactions and processes The compound's versatility allows it to be used in numerous chemical reactions and processes, making it a valuable asset in the synthesis of various products.
Check Digit Verification of cas no
The CAS Registry Mumber 90539-84-7 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 90539-84:
(7*9)+(6*0)+(5*5)+(4*3)+(3*9)+(2*8)+(1*4)=147
147 % 10 = 7
So 90539-84-7 is a valid CAS Registry Number.
90539-84-7Relevant articles and documents
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.
