5379-79-3 Usage
General Description
Indol-1-ylmethyl-dimethyl-amine, also known as 1-(Indol-1-yl)-N,N-dimethyl-methanamine, is a chemical compound with the molecular formula C13H16N2. It is an indole derivative and a tertiary amine that is primarily used as an intermediate in organic synthesis. The compound is characterized by its indole ring, which is a heterocyclic aromatic structure that is commonly found in many natural products and pharmaceuticals. Indol-1-ylmethyl-dimethyl-amine has potential applications in the development of new drugs due to its biological activity and interactions with specific receptors in the body. Additionally, it can be used as a building block for the synthesis of various organic compounds, making it a valuable tool in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 5379-79-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5379-79:
(6*5)+(5*3)+(4*7)+(3*9)+(2*7)+(1*9)=123
123 % 10 = 3
So 5379-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2/c1-12(2)9-13-8-7-10-5-3-4-6-11(10)13/h3-8H,9H2,1-2H3
5379-79-3Relevant articles and documents
Mild microwave-assisted synthesis of dipyrromethanes and their analogues
Xiong, Ruisheng,Borbas, K. Eszter
supporting information, p. 484 - 488 (2015/04/14)
The Mannich reaction between pyrroles or indoles and Eschenmoser's salt (dimethylmethylideneammonium iodide) forms N,N-dimethylamino-methylated derivatives in good to excellent yields. The reaction is highly regioselective, and for pyrroles both 2-and 3-s
An Alternative Route to 2-Substituted Indoles via N-Aminal-Directed Lithiation
Katritzky, Alan R.,Lue, Ping,Chen, Ya-Xiong
, p. 3688 - 3691 (2007/10/02)
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