104711-29-7 Usage
Molecular Weight
191.21 g/mol The molecular weight is the mass of one mole of the compound, which is calculated by adding the atomic weights of all the atoms in the molecular formula.
Structure
1H-Indole-2-carboxylic acid, 3-methyl-, methyl ester The structure of the compound is a derivative of 1H-indole-2-carboxylic acid with a methyl group added at the 3-position of the indole ring and an ester group (COOCH3) attached to the carboxylic acid (COOH) functional group.
Stability
Increased stability due to the presence of a methyl ester The addition of a methyl group at the 3-position of the indole ring increases the stability of the compound by introducing steric hindrance and reducing the electron density of the ring.
Solubility
Increased solubility due to the presence of a methyl ester The presence of the ester group (COOCH3) increases the polarity of the compound, which improves its solubility in organic solvents.
Pharmaceutical Applications
Used in the synthesis of various pharmaceuticals and bioactive compounds The compound is commonly used in the pharmaceutical industry as a building block for the synthesis of various heterocyclic compounds and has potential therapeutic properties, including anti-inflammatory and anti-cancer activities.
Research Reagent
Commonly used as a research reagent in the development of new drugs and pharmaceuticals The compound is often used in research and development as a starting material for the synthesis of new drugs and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 104711-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,1 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104711-29:
(8*1)+(7*0)+(6*4)+(5*7)+(4*1)+(3*1)+(2*2)+(1*9)=87
87 % 10 = 7
So 104711-29-7 is a valid CAS Registry Number.
104711-29-7Relevant articles and documents
Visible-Light-Induced Direct Photocatalytic Carboxylation of Indoles with CBr4/MeOH
Yang, Qing-Qing,Marchini, Marianna,Xiao, Wen-Jing,Ceroni, Paola,Bandini, Marco
, p. 18052 - 18056 (2015)
Photocatalysis enables the cascade reactions of indoles and CBr4 in MeOH through a C(sp2)-H functionalization/methanolysis sequence. The title reaction provides an efficient access to indole 2- and 3-carboxylates in a single operation (no preinstallation of protecting as well as directing groups was required) with good yields under mild reaction conditions. Shedding light on indole: The regioselective alkoxycarboxylation of indoles and heteroarenes using the CBr4/MeOH couple was accomplished through visible-light-induced photoredox catalysis. The described photocatalytic strategy features operational simplicity as well as high functional-group tolerance and represents a direct procedure to access indole carboxylates in generally moderate to good yields (see scheme).
