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4-((1H-indol-1-yl)methyl)morpholine is a chemical compound with the molecular formula C12H14N2O. It is a derivative of morpholine, an organic heterocyclic compound, and features an indole group attached to the morpholine ring through a methylene bridge. 4-((1H-indol-1-yl)methyl)morpholine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. Its structure provides a unique combination of properties that can be exploited in medicinal chemistry, such as its ability to form hydrogen bonds and its potential to act as a chiral auxiliary in asymmetric synthesis. The compound's specific role in these applications is determined by its reactivity, stability, and interaction with biological targets, making it a subject of interest in the field of chemical research and development.

5379-86-2

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5379-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5379-86-2 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, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5379-86:
(6*5)+(5*3)+(4*7)+(3*9)+(2*8)+(1*6)=122
122 % 10 = 2
So 5379-86-2 is a valid CAS Registry Number.

5379-86-2Downstream Products

5379-86-2Relevant academic research and scientific papers

Hf(OTf)4-Catalyzed regioselective N -aminomethylation of indoles and related NH-containing heterocycles

Sakai, Norio,Shimamura, Kazuyori,Ikeda, Reiko,Konakahara, Takeo

supporting information; experimental part, p. 3923 - 3926 (2010/07/05)

Figure presented Under Lewis acidic conditions using Hf(OTf)4, the aminomethylation of an indole derivative with a typical N,O-acetal preferentially produced kinetically favored N-aminomethylated indole derivatives instead of thermodynamically favored 3-aminomethylated indoles.

A general synthesis of 1-(dialkylaminomethyl)indoles

Love, Brian E.,Nguyen, Binh T.

, p. 1123 - 1125 (2007/10/03)

1-(N,N-Dialkylamino)methylindoles are prepared from the corresponding 1-(dialkylaminomethyl)benzotriazoles by treatment with indole and base. The aminoalkylation proceeds in high yield with good regioselectivity.

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