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(2-Methoxy-ethyl)-(5-methyl-furan-2-ylmethyl)-amine is a chemical compound with a molecular formula C9H13NO2. It is a derivative of furan and contains an amine group. (2-Methoxy-ethyl)-(5-methyl-furan-2-ylmethyl)-amine is known for its unique structure and reactivity, making it a versatile and important compound in various fields of science and industry.

106027-47-8

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106027-47-8 Usage

Uses

Used in Pharmaceutical Industry:
(2-Methoxy-ethyl)-(5-methyl-furan-2-ylmethyl)-amine is used as a building block in the development of new drugs due to its potential biological activity. Its unique structure and reactivity allow it to be a key component in the synthesis of pharmaceuticals.
Used in Agrochemical Industry:
(2-Methoxy-ethyl)-(5-methyl-furan-2-ylmethyl)-amine is also used in the synthesis of agrochemicals, contributing to the development of new and effective products for agricultural applications.
Used in Organic Chemistry Research:
Due to its unique structure and reactivity, (2-Methoxy-ethyl)-(5-methyl-furan-2-ylmethyl)-amine has potential applications in the field of organic chemistry research, where it can be utilized to explore new reactions and mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 106027-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,2 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106027-47:
(8*1)+(7*0)+(6*6)+(5*0)+(4*2)+(3*7)+(2*4)+(1*7)=88
88 % 10 = 8
So 106027-47-8 is a valid CAS Registry Number.

106027-47-8Downstream Products

106027-47-8Relevant academic research and scientific papers

A Facile Reduction of Certain Schiff Bases with Di- and Trichlorosilanes

Okamoto, Hidenori,Kato, Shozo

, p. 3466 - 3467 (1991)

The reduction of N--2,6-dimethylaniline (2) by use of trichlorosilane proceeded smoothly in the presence of a catalytic amount of BF3*Et2O.The trichlorosilane/BF3*Et2O combination was applicable to the reduction of various Schiff bases.In the case of dichlorosilane, the reduction of 2 proceeded with a 90percent yield without any catalysts.

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