19099-56-0 Usage
Uses
Used in Organic Synthesis:
3-Iodoisopropylbenzene is used as a reagent in organic synthesis for its ability to participate in nucleophilic substitution and other synthetic pathways. Its unique structure allows it to be a versatile building block in the creation of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3-Iodoisopropylbenzene is used as a key intermediate in the synthesis of various pharmaceuticals. Its role in the production process is to provide a starting material or a building block for the development of new drugs and medicinal compounds.
Used in Agrochemical Production:
3-Iodoisopropylbenzene also finds application in the agrochemical sector, where it is used in the synthesis of agrochemicals. It serves as a precursor in the production of pesticides, herbicides, and other agricultural chemicals, contributing to the development of effective solutions for crop protection.
Used in the Production of Fine Chemicals:
In the fine chemicals industry, 3-Iodoisopropylbenzene is employed as a building block for the synthesis of specialty chemicals. Its unique properties make it suitable for the production of high-value chemicals used in various applications, such as fragrances, dyes, and other specialty products.
Check Digit Verification of cas no
The CAS Registry Mumber 19099-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,9 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19099-56:
(7*1)+(6*9)+(5*0)+(4*9)+(3*9)+(2*5)+(1*6)=140
140 % 10 = 0
So 19099-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11I/c1-7(2)8-4-3-5-9(10)6-8/h3-7H,1-2H3
19099-56-0Relevant academic research and scientific papers
Synthesis of Azepino[1,2-a]indole-10-amines via [6+1] Annulation of Ynenitriles with Reformatsky Reagent
Iioka, Ryoya,Yorozu, Kohei,Sakai, Yoko,Kawai, Rika,Hatae, Noriyuki,Takashima, Katsuki,Tanabe, Genzoh,Wasada, Hiroaki,Yoshimatsu, Mitsuhiro
supporting information, p. 1553 - 1558 (2021/02/26)
Lewis acid-catalyzed [6+1] annulation reactions of 2-cyano-1-propargyl- and 2-alkynyl-1-cyanomethyl-indoles with Reformatsky reagent are described. 8-Aryl, 8-alkyl-, 8-hetaryl-, 9-aryl, and 9-alkyl-azepino[1,2-a]indole amines were obtained through a 7-endo-mode cyclization of the β-aminoacrylate intermediates. The antiproliferative activity of the azepino[1,2-a]indoles analogs against the HCT-116 cells were also examined.
