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N-<2-(2-furyl)ethyl>benzamide is a chemical compound with the molecular formula C12H13NO2. It is a derivative of benzamide, featuring a furylethyl group attached to the nitrogen atom. N-<2-(2-furyl)ethyl>benzamide is characterized by its potential applications in pharmaceutical research, particularly in the development of drugs targeting the central nervous system. Its structure, which includes a benzene ring and a furyl ring, may contribute to its interaction with biological targets. While the specific uses and mechanisms of action are not detailed here, the compound's unique structure suggests it may have properties that are of interest in medicinal chemistry.

5669-02-3

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5669-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5669-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5669-02:
(6*5)+(5*6)+(4*6)+(3*9)+(2*0)+(1*2)=113
113 % 10 = 3
So 5669-02-3 is a valid CAS Registry Number.

5669-02-3Relevant academic research and scientific papers

ORGANIC METAL COMPOUND, ORGANIC LIGHT-EMITTING DEVICES EMPLOYING THE SAME

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Paragraph 0050, (2017/07/26)

Organic metal compounds, and organic light-emitting devices employing the same are provided. The organic metal compound has a chemical structure represented by formula (I): wherein each R1 is independent and can be hydrogen, C1-12 al

A Robust, Recyclable Resin for Decagram Scale Resolution of (±)-Mefloquine and Other Chiral N-Heterocycles

Kreituss, Imants,Chen, Kuang-Yen,Eitel, Simon H.,Adam, Jean-Michel,Wuitschik, Georg,Fettes, Alec,Bode, Jeffrey W.

supporting information, p. 1553 - 1556 (2016/02/12)

Decagram quantities of enantiopure (+)-mefloquine have been produced via kinetic resolution of racemic mefloquine using a ROMP-gel supported chiral acyl hydroxamic acid resolving agent. The requisite monomer was prepared in a few synthetic steps without chromatography and polymerization was safely performed on a >30 gram scale under ambient conditions. The reagent was readily regenerated and reused multiple times for the resolution of 150 grams of (±)-mefloquine and other chiral N-heterocylces.

Studies on cerebral protective agents. X. Synthesis and evaluation of anticonvulsant activities for novel 4,5,6,7-tetrahydrothieno[3,2-c]pyridines and related compounds

Ohkubo, Mitsuru,Kuno, Atsushi,Katsuta, Kiyotaka,Ueda, Yoshiko,Shirakawa, Kiyoharu,Nakanishi, Hajime,Kinoshita, Takayoshi,Takasugi, Hisashi

, p. 778 - 784 (2007/10/03)

Novel 4,5,6,7-tetrahydrothieno[3,2-c]pyridines, 1-thienyl-1,2,3,4-tetrahydroisoquinolines and related compounds, in which the benzene rings of (+)- 1 (FR115427) were replaced with heteroaromatic rings such as thiophene, furan, benzothiophene and indole, w

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