104291-63-6 Usage
Uses
Used in Pharmaceutical Synthesis:
2-formyl-1H-indole-6-carbonitrile is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to react with a wide range of reagents, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-formyl-1H-indole-6-carbonitrile is utilized as a building block in the creation of novel agrochemicals, such as pesticides and herbicides, due to its unique chemical properties and reactivity.
Used in Organic Synthesis:
2-formyl-1H-indole-6-carbonitrile is employed as a versatile reactant in organic synthesis, allowing for the formation of various organic compounds through its reactivity with different chemical groups.
Used in Material Science:
2-formyl-1H-indole-6-carbonitrile may also find applications in material science, where its unique structure and properties can be harnessed to develop new materials with specific characteristics for various industrial uses.
Check Digit Verification of cas no
The CAS Registry Mumber 104291-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,9 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104291-63:
(8*1)+(7*0)+(6*4)+(5*2)+(4*9)+(3*1)+(2*6)+(1*3)=96
96 % 10 = 6
So 104291-63-6 is a valid CAS Registry Number.
104291-63-6Relevant academic research and scientific papers
Potent and broad-spectrum antibacterial activity of indole-based bisamidine antibiotics: Synthesis and SAR of novel analogs of MBX 1066 and MBX 1090
Williams, John D.,Nguyen, Son T.,Gu, Shen,Ding, Xiaoyuan,Butler, Michelle M.,Tashjian, Tommy F.,Opperman, Timothy J.,Panchal, Rekha G.,Bavari, Sina,Peet, Norton P.,Moir, Donald T.,Bowlin, Terry L.
, p. 7790 - 7806 (2014/01/06)
The prevalence of drug-resistant bacteria in the clinic has propelled a concerted effort to find new classes of antibiotics that will circumvent current modes of resistance. We have previously described a set of bisamidine antibiotics that contains a core
Synthesis of Antileukemic Indolylvinyl-1-benzofurans and -benzothiophenes
Dann, Otto,Char, Helmut,Fleischmann, Paul,Fricke, Helmut
, p. 438 - 455 (2007/10/02)
2--1-benzofuran and -benzothiophene compounds 6-13 and 18-22 with terminal amidinium or imidazolinium groups were synthesized; in their antileukemic activity in mice they surpass the isosteric 2,2'-vinylenebis(1-benzofuran) and -(benzo-thiophene) compounds.
