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2-(5-methoxy-1H-indol-3-yl)-2-(piperidin-1-yl)acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1000058-15-0

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1000058-15-0 Usage

Chemical structure

2-(5-methoxy-1H-indol-3-yl)-2-(piperidin-1-yl)acetonitrile is a complex organic compound consisting of an indole group with a methoxy substituent at the 5th position and a piperidine group connected to an acetonitrile group.

Indole group

The compound contains an indole group, which is a bicyclic aromatic system with a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Piperidine group

The compound also features a piperidine group, which is a six-membered heterocyclic ring system containing one nitrogen atom and five carbon atoms.

Acetonitrile group

The piperidine group is connected to an acetonitrile group (-CH2CN), which is a cyano group (C≡N) bonded to a methylene group (-CH2).

Potential applications

2-(5-methoxy-1H-indol-3-yl)-2-(piperidin-1-yl)acetonitrile has potential applications in the field of medicinal chemistry and drug development.

Interaction with biological targets

The compound's structural features may allow it to interact with biological targets such as receptors or enzymes, which could lead to potential pharmacological properties.

Further research needed

More research and investigation are required to fully understand the pharmacological properties and potential uses of 2-(5-methoxy-1H-indol-3-yl)-2-(piperidin-1-yl)acetonitrile.

Check Digit Verification of cas no

The CAS Registry Mumber 1000058-15-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,0,5 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1000058-15:
(9*1)+(8*0)+(7*0)+(6*0)+(5*0)+(4*5)+(3*8)+(2*1)+(1*5)=60
60 % 10 = 0
So 1000058-15-0 is a valid CAS Registry Number.

1000058-15-0Downstream Products

1000058-15-0Relevant academic research and scientific papers

A practical approach to non-natural or N-unsubstituted α-arylglycine derivatives: Hf(OTf)4-doped Me3SiCl system-catalyzed aminomethylation of electron-rich arenes with a new type of N,O-acetal

Sakai, Norio,Asano, Junichi,Shimano, Yuta,Konakahara, Takeo

, p. 9208 - 9215 (2008/12/21)

The authors have demonstrated the Hf(OTf)4-doped Me3SiCl system-catalyzed aminomethylation of electron-rich aromatic compounds, such as indoles and anilines, with new types of N,O-acetals having a variety of functional groups, such a

Hf(OTf)4-doped Me3SiCl-catalyzed aminomethylation of arenes with N,O-acetals: Facile approach to non-natural aromatic amino acid precursors

Sakai, Norio,Asano, Junichi,Shimano, Yuta,Konakahara, Takeo

, p. 2675 - 2678 (2008/02/11)

The authors demonstrated a Hf(OTf)4-Me3SiCl-system- catalyzed aminomethylation of an aromatic compound, such as a heterocycle or an electron-rich arene, with several new types of N,O-acetals having both a cyano group and a cyclic ami

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