881040-29-5 Usage
Uses
Used in Pharmaceutical Synthesis:
Dimethyl indole-2,6-dicarboxylate is used as a building block in the synthesis of pharmaceuticals and organic compounds, contributing to the development of new drugs and chemical entities.
Used in Fluorescence Probes for Nucleic Acid Detection:
Dimethyl indole-2,6-dicarboxylate is used as a fluorescence probe for the detection of nucleic acids, offering a potential tool for research and diagnostic applications in molecular biology.
Used in Dermatological Applications:
Dimethyl indole-2,6-dicarboxylate is used as a potential photo-protective agent in dermatological applications, providing a means to protect the skin from harmful UV radiation and related damage.
Used in Research and Development:
Dimethyl indole-2,6-dicarboxylate is utilized in research and development for exploring its biological activity and potential medicinal applications, furthering our understanding of its therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 881040-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,0,4 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 881040-29:
(8*8)+(7*8)+(6*1)+(5*0)+(4*4)+(3*0)+(2*2)+(1*9)=155
155 % 10 = 5
So 881040-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO4/c1-16-11(14)8-4-3-7-5-10(12(15)17-2)13-9(7)6-8/h3-6,13H,1-2H3
881040-29-5Relevant academic research and scientific papers
CuI-catalyzed intramolecular cyclization of 3-(2-aminophenyl)-2- bromoacrylate: Synthesis of 2-carboxyindoles
Xiao, Xiong,Chen, Tian-Qi,Ren, Jiangmeng,Chen, Wei-Dong,Zeng, Bu-Bing
, p. 2056 - 2060 (2014/04/03)
A new approach was described for the synthesis of substituted 2-carboxyindole using 3-(2-aminophenyl)-2-bromo-acrylates through a CuI-catalyzed intramolecular coupling. The reactions were mild, rapid and with good to excellent yields.
Tandem palladium-catalyzed N,C-coupling/carbonylation sequence for the synthesis of 2-carboxyindoles
Vieira, Tiago O.,Meaney, Laura A.,Shi, Yong-Ling,Alper, Howard
supporting information; experimental part, p. 4899 - 4901 (2009/05/31)
(Chemical Equation Presented) Tandem palladium-catalyzed N,C-coupling/carbonylation, under 10 aim of carbon monoxide and at 110 °C, is a novel and efficient method for the preparation of 2-carboxyindoles. The catalyst system tolerates a variety of functional groups, and the noted indoles were obtained in good isolated yields.
