881040-29-5 Usage
General Description
Dimethyl indole-2,6-dicarboxylate is a chemical compound with the molecular formula C12H12O4N2. It is a dimethyl ester derivative of indole-2,6-dicarboxylic acid and is commonly used as a building block in the synthesis of pharmaceuticals and organic compounds. Dimethyl indole-2,6-dicarboxylate exhibits potential biological activity and is being studied for its potential medicinal applications. Dimethyl indole-2,6-dicarboxylate has also been investigated for its potential as a fluorescence probe for nucleic acid detection and as a potential photo-protective agent in dermatological applications. It is important to handle this compound with care, as it may pose risks to human health and the environment.
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 articles and documents
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.
