161532-19-0 Usage
Ester derivative
1H-Indole-3-carboxylic acid, 4-methoxy-, methyl ester is an ester derivative of 1H-indole-3-carboxylic acid, indicating the presence of an ester functional group (-COO-) in its structure.
Methoxy group attachment
The compound contains a methoxy group (-OCH3) attached to the fourth carbon of the indole ring, which influences its chemical properties and reactivity.
Organic synthesis and pharmaceutical research
1H-Indole-3-carboxylic acid, 4-methoxy-, methyl ester is commonly used as a building block in organic synthesis and pharmaceutical research for the production of various chemical compounds.
Potential applications in medicinal chemistry
This compound has potential applications in medicinal chemistry, particularly in drug discovery and development, due to its unique structure and properties.
Biological activity
1H-Indole-3-carboxylic acid, 4-methoxy-, methyl ester may exhibit biological activity, which could make it useful as a precursor for the synthesis of bioactive molecules.
Starting material for diverse molecular structures
The compound's structural features make it a suitable starting material for the preparation of diverse molecular structures with varied properties and applications, expanding its utility in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 161532-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,3 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 161532-19:
(8*1)+(7*6)+(6*1)+(5*5)+(4*3)+(3*2)+(2*1)+(1*9)=110
110 % 10 = 0
So 161532-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c1-14-9-5-3-4-8-10(9)7(6-12-8)11(13)15-2/h3-6,12H,1-2H3
161532-19-0Relevant articles and documents
A general and scalable synthesis of polysubstituted indoles
Diana-Rivero, Raquel,García-Tellado, Fernando,Tejedor, David
, (2021/06/14)
A consecutive 2-step synthesis of N-unprotected polysubstituted indoles bearing an electron-withdrawing group at the C-3 position from readily available nitroarenes is reported. The protocol is based on the [3,3]-sigmatropic rearrangement of N-oxyenamines generated by the DABCO-catalyzed reaction of N-arylhydroxylamines and conjugated terminal alkynes, and delivers indoles endowed with a wide array of substitution patterns and topologies.
